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. 2016 Nov 12;136(1):107–118. doi: 10.1007/s00439-016-1746-7

A common variant in CLDN14 causes precipitous, prelingual sensorineural hearing loss in multiple families due to founder effect

Justin A Pater 1, Tammy Benteau 1, Anne Griffin 1, Cindy Penney 1, Susan G Stanton 2, Sarah Predham 1, Bernadine Kielley 3, Jessica Squires 1, Jiayi Zhou 1, Quan Li 1, Nelly Abdelfatah 1, Darren D O’Rielly 1,4, Terry-Lynn Young 1,2,4,✉
PMCID: PMC5215284  PMID: 27838790

Abstract

Genetic isolates provide unprecedented opportunities to identify pathogenic mutations and explore the full natural history of clinically heterogeneous phenotypes such as hearing loss. We noticed a unique audioprofile, characterized by prelingual and rapid deterioration of hearing thresholds at frequencies >0.5 kHz in several adults from unrelated families from the island population of Newfoundland. Targeted serial Sanger sequencing of probands for deafness alleles (n = 23) that we previously identified in this founder population was negative. Whole exome sequencing in four members of the largest family (R2010) identified a CLDN14 (DFNB29) variant [c.488C>T; p. (Ala163Val)], likely pathogenic, sensorineural hearing loss, autosomal recessive. Although not associated with deafness or disease, CLDN14 p.(Ala163Val) has been previously reported as a variant of uncertain significance (VUS). Targeted sequencing of 169 deafness probands identified one homozygote and one heterozygous carrier. Genealogical studies, cascade sequencing and haplotype analysis across four unrelated families showed all subjects with the unique audioprofile (n = 12) were also homozygous for p.(Ala163Val) and shared a 1.4 Mb DFNB29-associated haplotype on chromosome 21. Most significantly, sequencing 175 population controls revealed 1% of the population are heterozygous for CLDN14 p.(Ala163Val), consistent with a major founder effect in Newfoundland. The youngest CLDN14 [c.488C>T; p.(Ala163Val)] homozygote passed newborn screening and had normal hearing thresholds up to 3 years of age, which then deteriorated to a precipitous loss >1 kHz during the first decade. Our study suggests that genetic testing may be necessary to identify at-risk children in time to prevent speech, language and developmental delay.

Electronic supplementary material

The online version of this article (doi:10.1007/s00439-016-1746-7) contains supplementary material, which is available to authorized users.

Introduction

Hearing loss is one of the most common and genetic of all human phenotypes. Permanent bilateral sensorineural hearing loss affects 1/500 newborns, and almost twice as many adolescents (Smith et al. 1999; Morton and Nance 2006). Although approximately two-thirds of prelingual severe hearing loss cases are recessive, and 94 deafness loci have been reported, only a minority of hearing loss cases with a presumed recessive inheritance pattern can be conclusively diagnosed with a clear genetic etiology (Sloan-Heggen et al. 2016). Therefore, many recessive cases may be due to genetic defects in genes yet to be identified. However, recent studies using new high-throughput technologies and broader application in multi-ethnic populations report GJB2 yields of less than 25%, suggesting a larger role for other recessive genes in prelingual severe cases (Yan et al. 2016; Sloan-Heggen et al. 2016).

Sensorineural hearing loss is characterized by both degree (mild, moderate, severe or profound) and configuration (low, mid and/or high frequency) using the standard behavioral audiogram. Although clinically heterogeneous, rare pathognomonic audiograms may present with surprising regularity in clinics within genetically isolated populations and where patients often share a common ancestor due to founder effects. For example, the Finnish and Pakistani populations have been invaluable for discovery of deafness genes as population bottlenecks (genetic drift) and/or inbreeding increase the likelihood of inheriting recessive alleles that are identical by descent. These populations are often characterized by large sibships, deep genealogies and higher consanguineous rates. The population of Newfoundland and Labrador (NL) was founded by ~20,000 Protestant English and Roman Catholic Irish settlers. Religious and geographic isolation within small coastal fishing (outport) communities (Manion 1977) has resulted in a higher inbreeding coefficient in the NL population (Bear et al. 1987, 1988; Zhai et al. 2015). We have previously identified several founder deafness mutations in the NL populations (Abdelfatah et al. 2013a, b; Ahmed et al. 2004; Doucette et al. 2009; Young et al. 2001).

A unique clinical audioprofile of steeply sloping sensorineural hearing loss was noted in several unrelated families. Herein, we report a founder missense variant in CLDN14 causing precipitous prelingual sensorineural hearing loss in children born with normal hearing thresholds. The essential role of CLDN14, a component of tight junctions, was first discovered through studies in consanguineous families from the genetically isolated population of Pakistan. Tight junctions have been shown to play a significant role in maintaining the structural integrity of cells within the inner ear. Other genes encoding tight junction proteins, such as MARVELD2 (DFNB49) (Riazuddin et al. 2006; Nayak et al. 2016), have also been implicated in recessive hearing loss. Claudin-14 is essential for the formation of tight junctions and is expressed in both hair cells and supporting cells of the organ of Corti; however, CLDN14 exhibits preferential gene expression in sensory hair cells over supporting cells (Wilcox et al. 2001; Ben-Yosef et al. 2003; Scheffer et al. 2015). Initially, CLDN14 was considered the cause of congenital recessive and profound deafness (Wilcox et al. 2001), and more recently of milder forms of hearing loss (Bashir et al. 2013). The CLDN14 c. 488C>T p.(Ala163Val) allele has previously been reported in multiple studies as a variant of uncertain significance (VUS; Thorleifsson et al. 2009; Toka et al. 2013; Purcell et al. 2014) and recently identified by Sloan-Heggen et al. (2016) as one of two VUS in a patient with congenital hearing loss. Our study shows children inheriting two copies of CLDN14 c. 488C>T p.(Ala163Val) alleles are born with normal hearing thresholds and experience a rapid and progressive loss by 3–4 years of age. Extensive clinical recruitment and targeted screening suggest that CLDN14 p.(Ala163Val) represents a major founder variant in the Newfoundland population.

Materials and methods

Study participants and audiometric evaluations

This project is part of a large study of hereditary hearing loss in the Canadian province of Newfoundland and Labrador. Informed consent, family history and permission to access medical records and audiograms were obtained from all participants as per approved institutional review board protocol #01.186 (Human Research Ethics Board, St. John’s, NL, Canada). Sensorineural hearing loss was determined when hearing thresholds were abnormal, and the air and bone conduction results within 10 decibels (dB) of each other (i.e., air–bone gaps of 10 dB or less). Both retrospective and prospective audiograms and health records were obtained.

In the course of ongoing clinical recruitment, we noted a rare but consistent clinical audioprofile characterized as steeply sloping, sensorineural hearing loss above 0.5 kHz with mid- and high-frequency thresholds in the severe to profound range (Fig. 1a–d). On the premise that subjects with this hearing loss pattern also shared a recent common ancestor, we used the distinct audioprofile to guide clinical recruitment, and a research team visited several small fishing villages (outports) to measure hearing thresholds, extend pedigrees, provide genetic counseling and collect blood samples (Fig. 2).

Fig. 1.

Fig. 1

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Rare, precipitous audiologic phenotype caused by CLDN14 (c.488C>T; p.(Ala163Val)) in an Irish clan. a Pure tone audiogram of Family 2010 proband (PID V-9) and sister (PID V-10), b pure tone audiogram series for PID VI-2 (Family 2075) showing normal hearing at age 2 years and a progressive hearing loss apparent by 4 years of age, c first and d second decade pure tone audiogram of affected subjects. Yellow shaded area indicates range of normal hearing. Hearing thresholds are measured in decibels hearing level (dB HL), X = left ear (air conduction), O = right ear (air conduction), > = left ear (bone conduction), ↘ = no response at the limits of the audiometer. * = 8 kHz was not measured

Fig. 2.

Fig. 2

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Combined pedigrees of three families (2033, 2075 and 2010) with rare, precipitous audiologic phenotype connect to a founding couple and share an ancestral DFNB29-associated haplotype. Shaded symbols precipitous sensorineural hearing loss. Half-shaded symbols unspecified hearing loss

DNA preparation, targeted sequencing and audioprofiling

Genomic DNA was extracted from peripheral blood using a simple salting out protocol (Miller et al. 1988). All probands recruited to the study were screened for population-specific deafness alleles (Supplementary Table 1; Abdelfatah et al. 2013a, b; Ahmed et al. 2004; Doucette et al. 2009; Young et al. 2001). To identify other candidate genes to screen, audiograms were submitted to Audiogene (Hildebrand et al. 2009) for computerized comparison with known average audiograms of 16 autosomal dominant loci (under the assumption that hearing loss was segregating as an autosomal dominant trait in these NL families). Bidirectional Sanger sequencing (ABI PRISM 3500XL DNA Analyzer; Applied Biosystems, Foster City, CA, USA) with standard PCR assay using Primer3 (Untergasser et al. 2012) was used to screen candidate mutations and genes (Merner et al. 2008). We used Mutation Surveyor Software (version 4.07, SoftGenetics LLC State College, PA 16803) to select quality reads and analyze DNA sequences.

Whole exome sequencing and variant filtration

We prepared whole exome libraries for four members of Family 2010 using the Ion Torrent AmpliSeq RDY Exome Kit (Life Technologies, Cat. #A27193) (Fig. 2). Exome library purification, adapter ligation and barcoding were done using the Ion PI Hi-Q OT2 200 kit (Life Technologies, Cat. #A26434). Purified libraries were quantified using the Ion Library Quantification Kit (Life Technologies, Cat. #4468802) and then loaded onto a PI v3 chip and sequenced with the Ion Torrent Proton Sequencer. Single-nucleotide variants (SNVs) and insertion/deletions (INDELs) were called (GATK, v3.5) and annotated using SnpEff (v4.1; http://snpeff.sourceforge.net/) and SNVs were filtered against publically available SNP databases (ExAC Browser, http://exac.broadinstitute.org/; dbSNP, http://www.ncbi.nlm.nih.gov/projects/SNP/; 1000 genomes, http://www.1000genomes.org). We assessed the impact of SNVs at the protein level with SIFT, PolyPhen-2, and MutationTaster. Filtered SNVs had a minimum of 20× coverage, a predicted moderate/high impact (nonsense, frameshift, missense, splice sites) and a minor allele frequency (MAF) of <1%. The apparent vertical transmission of hearing loss in several branches of the clan pedigree (Fig. 2) could be due to either a dominant gene with reduced penetrance, or a recessive gene with a pseudodominant inheritance pattern; therefore, we conducted both autosomal dominant and recessive analyses.

Cascade sequencing and haplotype analysis

Potential pathogenic mutations were subjected to cascade screening in all available relatives across three families observed to have the same rare audioprofile (Families 2010, 2033 and 2075) and also in 175 ethnically matched controls. Microsatellites flanking candidate genes were genotyped according to standard procedures (Abdelfatah et al. 2013a) and alleles called using GeneMapper software v4.0. Haplotypes were reconstructed manually and compared across families. Variants of interest were also screened in 169 deafness probands with Newfoundland ancestry.

Results

Clinical evaluation

Our research audiologist (AG) noted that probands (from Families 2010, 2075 and 2033) all shared a unique hearing loss pattern. The proband of Family 2010 (V-9; Fig. 2) presented at 36 years of age with the characteristic pattern of normal low-frequency thresholds, steeply sloping to severe bilateral, symmetrical, sensorineural hearing loss throughout mid and high frequencies (Fig. 1a). Age appropriate audiologic tests of the proband’s son (VI-4; Fig. 2) at 1 month and 1 year of age were normal. Serial audiograms on PID VI-2 (Fig. 1b; Family 2075) show normal hearing thresholds across frequencies up to 3 years of age, and subsequent rapid progression of hearing loss affecting high frequencies first. Significant hearing loss of variable severity is already present in children aged 5–7 years (Fig. 1c), which include probands of families 2033 and 2075. By the middle of the second decade of life, these children uniformly exhibit the distinctive steeply sloping audiogram (Fig. 1d). The hearing loss progresses slowly during subsequent decades, primarily in the mid–high frequencies, with relatively well-preserved low-frequency thresholds. For adults, some variation in thresholds at 0.5 kHz is observed (PID V-10; Fig. 1a) but otherwise the adult presentation is relatively uniform.

Targeted sequencing and audioprofiling

Targeted sequencing was carried out on probands for known deafness alleles (previously identified in this population; Supplementary Table 1) but none were found. Several gene candidates, as suggested by Audiogene (Hildebrand et al. 2009), were also Sanger sequenced, including COCH, KCNQ4 and TMC1. We identified a rare variant in TMC1 (c.421C>T; MAF of 0.01%) predicted to cause the substitution of arginine to a tryptophan residue at position 141 and to be deleterious by SIFT (and probably damaging by PolyPhen-2 and Panther). Although identified in both the probands (V-11) of Family 2010 and transmitted to her affected son (V-14), the c.421C>T variant did not co-segregate with mid–high-frequency loss in this family (data not shown).

Whole exome sequencing

Whole exome sequencing on Family 2010 using three affecteds (V-9, VI-4 and V-17) and one unaffected parent (V-8) (Fig. 2) yielded >35,000 total variants. Under a dominant model, 34 heterozygous variants were filtered (data not shown). However, none of these variants resided within known deafness genes/loci (http://hereditaryhearingloss.org/). Under a recessive model, we filtered four homozygous variants (in PRKDC, ZNF404, CUL7 and CLDN14). One of these, CLDN14 (DFNB29) is a known deafness gene expressed in the sensory epithelium of the organ of Corti of the inner ear (Wilcox et al. 2001; Scheffer et al. 2015). CLDN14 consists of three exons and two isoforms and encodes a protein containing four transmembrane domains. The CLDN14 p.(Ala163Val) point variant (Fig. 3c) identified in Family 2010 predicts substitution of an alanine to a valine at the beginning of the fourth transmembrane domain (Fig. 4a) and is highly conserved (Fig. 3b). The CLDN14 c.488C>T allele was first identified in the Icelandic population (Thorleifsson et al. 2009). Globally, the CLDN14 c.488C>T variant has an MAF of 0.02564% (ExAC Browser, http://exac.broadinstitute.org/) and has been reported in both European and African populations. The heterozygous CLDN14 (human GRCh37/hg19: g. 37833506 G>A, NM_012130.3: c.488 C>T) allele is reported as a variant of uncertain significance in dbSNP (rs143797113), ExAC browser (MAF: 0.02564%), 1000 genomes (MAF: 0.04%), and the Grand Opportunity Exome Sequencing Project (MAF: 0.05%). This allele has also been reported in several control samples from other study cohorts within the USA (Toka et al. 2013), Sweden (Purcell et al. 2014), and Africa (ExAC browser). The majority of known pathogenic CLDN14 mutations reside within one of the transmembrane domains in Claudin-14 (Fig. 4a; Bashir et al. 2013; Charif et al. 2013; Lee et al. 2012; Wattenhofer et al. 2005; Wilcox et al. 2001). Functional studies of CLDN14 mutations have demonstrated the importance of transmembrane domains with respect to protein topology and folding, as well as proper spatial localization within cells. For example, previous localization experiments showed that the p.V85D and p. G101R deafness mutations within domain II (Fig. 4a) fail to form tight junctions due to the mislocalization of Claudin-14 protein to the cytoplasm, in vitro (Wattenhofer et al. 2005). Since p. (Ala163Val) is predicted to change a highly conserved amino acid within the fourth transmembrane domain (Fig. 3b), we suspect a similar impact regarding the spatial localization of claudin-14 to the plasma membrane, leading to the cells’ inability to form tight junctions. While previous research have demonstrated the importance of amino acid conservation within in claudin-14 transmembrane domains, experimental functional studies are warranted to prove CLDN14 c.488C>T, p.(Ala163Val) pathogenicity.

Fig. 3.

Fig. 3

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a Pedigree of family R2072, identified in screening of the NL deafness cohort, with the rare, precipitous audiologic phenotype who also share the CLDN14 [c.488C>T; p.(Ala163Val)] variant and ancestral DFNB29-associated haplotype, b Conservation of the Claudin-14 protein using Clustal Omega and WebLogo display. Homo sapiens (NP_001139551.1), Pan paniscus (XP_008975916.1), Mus musculus (NP_001159398.1), Rattus norvegicus (NP_001013447.1), Canis lupus familiaris (XP_013965166.1), Gallus gallus (XP_015155717.1), Gekko japonicas (XP_015277878.1), Pelodiscus sinensis (XP_006126056.1), Xenopus laevis (NP_001086045.1), Danio rerio (NP_001004559.2). Red font and arrow indicate a highly conserved alanine residue at position 163, c sequence electropherograms of CLDN14 [c.488C>T; p.(Ala163Val)]. Box highlights variant, d wild-type/normal CLDN14 c.488C. Box highlights normal sequence

Fig. 4.

Fig. 4

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a Location of pathogenic mutations in Claudin-14. Colored amino acid residues indicate previously reported claudin-14 mutations. Arrow indicates position of CLDN14 c.488C>T [p.(Ala163Val)]. Adapted from: Bashir et al. (2013), b Cross-sectional diagram illustrating the anatomical location of the cochlear canals and their respective ionic composition. *CLDN14 expression, c Schematic diagram demonstrating the molecular structure of tight junctions

Cascade sequencing and haplotype analysis

Cascade sequencing in all available subjects from Families 2033 and 2075 show that affecteds with the distinct precipitous mid–high-frequency hearing loss (Fig. 2, filled symbols) were also homozygous for CLDN14 p.(Ala163Val) (Fig. 3c). Subjects with a flat loss, such as PID IV-4 and his descendants (V-5, V-7 and VI-4) lacked the recessive CLDN14 variant (Fig. 3d). This pattern is consistent with our hypothesis that CLDN14 p.(Ala163Val) is a likely pathogenic, recessive allele where homozygosity results in a distinct precipitous mid–high-frequency hearing loss and relatives inheriting a single copy (carriers) or wild type do not have this pattern. According to the American College of Medical Genetics standards and guideline (Richards et al. 2015), CLDN14 p.(Ala163Val) is a strong PS4 PM2 likely pathogenic variant. The cause of hearing loss in subjects with flat audioprofiles is not known, but is clearly not due to homozygosity for CLDN14 c.488C>T. Future studies will explore the genetic etiology of their hearing loss. Furthermore, screening our cohort of 169 deafness probands identified an additional homozygous subject (Family 2072) and two heterozygous carriers. In Family 2072, the proband’s mother (with the distinct audioprofile) was also found to be homozygous for CLDN14 p.(Ala163Val) and her father a carrier (Fig. 3a). Screening population controls identified four carriers out of 175 subjects, estimating an MAF of 1.15% in the Newfoundland population and suggesting that this likely pathogenic variant is not rare.

Extensive genotyping in the vicinity of DFNB29 revealed that p.(Ala163Val) resides on a 1.4 Mb ancestral haplotype shared across all four families (Figs. 2, 3a). Haplotype analysis shows affected individuals in the four families inherit an ancestral DFNB29-associated haplotype on chromosome 21q22.1, signifying clan membership, although biological connection for Family 2072 was not found (Fig. 3a). Additionally, we sequenced all coding sequences of the CLDN14 gene, including the exon/intron boundaries and 5′ and 3′ UTRs. We identified a common synonymous variant (c.243C>T; rs219799) within the clan, which was incorporated into our DFNB29-associated deafness haplotype.

Genealogical analysis

Extension of the pedigrees and review of all clinical audiograms identified 16 subjects with hearing loss; 10/16 subjects showed the distinct precipitous mid–high-frequency hearing loss (Fig. 2). Subjects with hearing impairment not consistent with the distinct precipitous mid–high-frequency pattern include PID IV-3 (whom we have not connected to the founding couple) and all descendants of PID IV-4 (Fig. 2). In these cases, the audiogram can be characterized as a flat loss across all frequencies: PID IV-4 had a profound flat loss and his descendants (V-5, V-7, VI-3) show a mild flat loss (Fig. 5). Family interviews determined the surnames suggestive of Irish descent (Seary 1977) and connected Families 2010, 2033 and 2075 to a single founding couple six generations ago. We noted that the inheritance pattern in the combined pedigree suggested either autosomal dominant (with reduced penetrance) or autosomal recessive (pseudodominant) inheritance (Fig. 2). In summary, this population-based study using a targeted and whole exome sequencing approach identified a CLDN14 (DFNB29) variant (c.488C>T, p. (Ala163Val), likely pathogenic, sensorineural hearing loss, autosomal recessive.

Fig. 5.

Fig. 5

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Clan members lacking the recessive CLDN14 [c.488C>T; p.(Ala163Val)] variant do not present with the characteristic steeply sloping hearing phenotype, exhibiting a different age of onset and hearing threshold progression a Profound, flat sensorineural hearing loss with an unknown etiology at age 63 (PID IV-4), b PID V-5 (age: 53) presents with borderline hearing thresholds, c PID V-7 (age: 58) presents with mild hearing loss with a diagnosis of Meniere’s disease, d at age 39, PID VI-3 presents with mild hearing loss, and e a heterozygous CLDN14 [c.488C>T; p.(Ala163Val)] carrier (PID V-4) exhibits mild hearing loss at age 60. Yellow shaded area indicates range of normal hearing. Hearing thresholds are measured in decibels hearing level (dB HL), X = left ear (air conduction), O = right ear (air conduction)

Discussion

We have determined that a known VUS (CLDN14, c.488C>T, p. (Ala163Val)) is likely pathogenic, and causes a precipitous, bilateral and rapid deterioration of hearing thresholds at frequencies >0.75 kHz in children, progressing gradually in adults. We have also determined that this likely pathogenic variant is amplified in the founder population of the island of Newfoundland and is present in ~1% of the population. The role of CLDN14 in nonsyndromic hearing loss was first described in two large consanguineous families from Pakistan with recessive profound congenital deafness (Wilcox et al. 2001). Recessive CLDN14 alleles manifest as nonsyndromic sensorineural hearing loss with considerable phenotypic variability and may present as congenital or prelingual, and mild, moderate–severe or profound (Bashir et al. 2010, 2013). In this study, homozygous children had normal hearing thresholds up to 3 years of age and overall, a remarkably conserved hearing phenotype. A combination of pedigree extension and genotyping linked four families of Irish ancestry to a founding couple six generations back.

The claudin family of proteins consists of 24 members with tissue-specific expression. Claudin-14 plays a critical role in the formation of tight junction barriers that regulate paracellular ion transport (Mineta et al. 2011) and is highly expressed in the kidney, liver and the inner ear (Ben-Yosef et al. 2003; Wilcox et al. 2001). Moreover, preferential gene expression has been observed in the inner ear, as CLDN14 expression is lower in supporting cells, relative to sensory hair cells (Wilcox et al. 2001; Scheffer et al. 2015). Normal hearing function and hair cell depolarization are dependent on tight junctions in the reticular lamina. In the organ of Corti, hair cell stereocilia are bathed in potassium-rich endolymph, while the basolateral surface of the hair cell body is surrounded by an intercellular (or extracellular) fluid continuous with the perilymph (Fig. 4b, c). The reticular lamina, formed in part by tight junctions between the apical surfaces of hair cells and supporting cells of the sensory epithelium, creates a barrier isolating the endolymphatic fluid from other cochlear compartments, which contain perilymph. Maintenance of this ionic gradient is essential for mechanotransduction, which depends on the modulation of potassium current flowing from the endolymph into the hair cells through the stereocilia as they are displaced by sound-induced vibrations. Disruption of this tight junction barrier alters the ionic gradient, increasing the potassium concentration around the hair cell body, compromising mechanotransduction and causing hair cell toxicity and eventual cell death.

The CLDN14 p.(Ala163Val) variant reported in this study has been identified in previous studies but not in association with disease. It was first reported as a VUS by Thorleifsson et al. (2009) in a large Iceland/Netherlands GWAS cohort study examining SNPs associated with kidney stones and bone mineral density and more recently by Toka et al. (2013), who detected the CLDN14 p.(Ala163Val) allele in 3 of 1230 study participants for another kidney function study. The heterozygous p.(Ala163Val) allele was also found in a Swedish GWAS study examining the polygenic nature of schizophrenia (Purcell et al. 2014). The heterozygous p.(Ala163Val) allele was submitted 31 times to ExAC browser, 29 alleles from European descent and 2 from the African population. In a recent American study including 1119 deafness probands, a cohort made up of 62.3% autosomal recessive cases (Sloan-Heggen et al. 2016) used a targeted sequencing approach and the most commonly implicated genes were GJB2, MYH9, OTOA, PCDH15, SLC26A4, STRC, TMC1, TMPRSS3 and USH2A. Interestingly, Sloan-Heggen et al. 2016 reported the p.(Ala163Val) allele in a patient with congenital hearing loss; however, in a compound heterozygous state with a second CLDN14 allele (p.P28L). In summary, these studies suggest that the likely pathogenic CLDN14 p.(Ala163Val) allele is both rare and widely distributed around the globe.

Many reports claim that approximately 50% of autosomal recessive deafness is caused by either homozygous or compound heterozygous mutations in the DFNB1 locus (GJB2), which is often the only gene that is routinely screened in the clinical setting when there is a family history of hearing loss. This represents a massive ascertainment bias, as children who are DFNB1 negative are not followed up, due to the expenses associated with genetic testing. Recently, a large, ethnically diverse, cohort study demonstrated the importance of investigating DFNB1-negative deaf probands (Yan et al. 2016). This study took a targeted panel approach in 342 probands (185 simplex and 157 multiplex families), sequenced 180 known hearing loss genes, and identified 151 variants in 119 families. Fifty-three families had pathogenic or likely pathogenic mutations within 27 genes, while the remaining were variants of uncertain significance. This study solved 25 and 7% of multiplex and simplex families, respectively, emphasizing the importance of large families and strong histories of disease in genetic studies.

Pediatric hearing programs strive to identify and treat early to prevent delay in language, learning and social development. However, the detection of delayed onset and progressive forms of hearing loss remain a significant challenge. Children who are homozygous CLDN14 p.(Ala163Val) pass newborn and early hearing tests. The proband’s son (R2010, PID VI-4) was discharged after his test at 1 year of age indicated normal hearing. Preschool testing 4 years later showed significant deterioration of both mid and high frequencies (Fig. 1c). Delayed identification could result from limited testing of high frequencies in the preschool years, often complicated by limited testing tolerance in children. In this study, PID VI-2 had normal hearing at 8 kHz at 2 years of age. At 3 years, hearing was reported normal although thresholds at 8 kHz were not performed. By 4 years, a 55 dBHL threshold at 8 kHz and mild to moderate loss at all high frequencies required immediate hearing aid fitting. Retrospectively, if 8 kHz thresholds had been performed at 3 years, diagnosis and therapy could have been offered a year earlier (Fig. 1b). Conversely, genetic testing or prenatal/preconception parental carrier screening could provide appropriate hearing surveillance and minimize the risk of delays in language development and learning from rapidly progressing hearing loss.

Adults who are homozygous for CLDN14 p.(Ala163Val) also have a consistent phenotype but challenges in management remain. Hearing aids benefit affected children and young adults (up to the third decade), but most adults do not find them beneficial. For example, PIDs V-9 (age: 50), V-10 (age: 51) and V-17 (age: 57; Fig. 2) reported some additional sound with hearing aids but no improvement of speech comprehension, consistent with the extreme erosion of mid and high frequencies. Older affected adults with well-preserved low-frequency sensitivity have limited communication by phone. PIDs V-10 and V-17 (Fig. 2) whose threshold at 0.5 kHz is deteriorated can no longer communicate by phone. Adult members of this clan are highly skilled speech readers who can detect speech initiation and turn quickly to maximize the use of visual clues. Unfortunately, these skills can be mistaken for hearing and subjects have voiced concerns regarding safety in the workplace.

The development of the organ of Corti is unidirectional, and follows a base-to-apex hair cell degeneration in the Cldn14-null mouse cochlea. This may explain why we observe a sensorineural threshold loss progressing from the high to low frequencies in affected clan members. The cochlea discerns high- from low-frequency sound, based on a stiffness gradient along the basilar membrane (Ehret 1978; Teudt and Richter 2014). In Cldn14-null mice, the organ of Corti undergoes a base-to-apex deterioration beginning around postnatal day 10, with a more severe and rapid degeneration of outer hair cells compared to inner hair cells. By day 13, the three rows of outer hair cells are almost completely absent in the cochlear base, with partial loss and stereociliar disorganization in the middle and apical turns (Ben-Yosef et al. 2003). The cochlear lesion then proceeds towards the cochlear apex, with a rapid deterioration of the outer hair cells accompanied by the onset of inner hair cell damage. By day 18, outer hair cell deterioration is severe with only a few remaining outer hair cells exhibiting damaged stereocilia in the most apical region; in contrast, only partial inner hair cell loss is reported throughout the cochlea by this age. Auditory brainstem responses measured in 4-week-old Cldn14-null mice indicate a significant hearing loss in comparison to their wild-type and heterozygous littermates (Ben-Yosef et al. 2003).

Summary

A population-based study of hearing loss in the NL population has clarified the role of CLDN14 p.(Ala163Val), a VUS previously identified in the USA, Iceland and Sweden. CLDN14 p.(Ala163Val) appears to be of Irish origin and causes a precipitous, prelingual recessive sensorineural hearing loss. This likely pathogenic variant is frequent in this island population of Northern European decent, and CLDN14 p.(Ala163Val) homozygotes have normal hearing thresholds at birth, then experience rapid, progressive nonsyndromic hearing loss in early childhood. Although missed by newborn hearing screening, genetic testing would ensure identification of at-risk children, allowing for appropriate monitoring and timely intervention, aural rehabilitation and counseling for families. Although GJB2 is routinely screened in the regional hospital diagnostic clinic, we recommend targeted screening of CLDN14, as well.

Limitations

While exome sequencing is a powerful tool to elucidate disease causing, coding variant, it does not explore non-coding regions. Additionally, there is no experimental proof of the predicted amino acid substitution, and without functional data, we cannot be certain that the point mutation impacts protein location within tight junctions. For example, this variant could cause alternative splicing or alter gene expression. Although less likely, it is plausible that a causal, non-coding variant at the DFNB29 locus is in linkage disequilibrium with p.(Ala163Val). Even though our study presents several lines of evidence to suggest pathogenicity, experimental functional analysis of p.(Ala163Val) is required.

Electronic supplementary material

Below is the link to the electronic supplementary material.

Supplementary material 1 (PDF 56 kb) (55.8KB, pdf)

Acknowledgements

We are grateful to the individuals who participated in this study and to Elspeth Drinkell, Carol Negrijn, Jim Houston and Dante Galutira for technical assistance.

Compliance with ethical standards

Funding

This work was supported by a grant from the Canadian Institutes for Health Research-Regional Partnership Program with the Research and Development Corporation of Newfoundland and Labrador, the Canadian Foundation for Innovation (New Investigator Award no. 9384 and Leaders Opportunity Fund no. 13120) and Genome Canada (Atlantic Medical Genetics and Genomics Initiative). The authors also gratefully acknowledge financial support from the Janeway Children’s Hospital Foundation, Memorial University and the Government of Newfoundland and Labrador. N.A. is a CIHR-RPP Fellowship awardee.

Conflict of interest

The authors declare that they have no conflict of interest.

References

  1. Abdelfatah N, McComiskey DA, Doucette L, Griffin A, Moore SJ, Negrijn C, Hodgkinson KA, King JJ, Larijani M, Houston J, Stanton SG, Young TL. Identification of a novel in-frame deletion in KCNQ4 (DFNA2A) and evidence of multiple phenocopies of unknown origin in a family with ADSNHL. Eur J Hum Genet. 2013;21:1112–1119. doi: 10.1038/ejhg.2013.5. [DOI] [PMC free article] [PubMed] [Google Scholar]
  2. Abdelfatah N, Merner N, Houston J, Benteau T, Griffin A, Doucette L, Stockley T, Lauzon JL, Young TL. A novel deletion in SMPX causes a rare form of X-linked progressive hearing loss in two families due to a founder effect. Hum Mutat. 2013;34:66–69. doi: 10.1002/humu.22205. [DOI] [PubMed] [Google Scholar]
  3. Ahmed ZM, Li XC, Powell SD, Riazuddin S, Young TL, Ramzan K, Ahmad Z, Luscombe S, Dhillon K, MacLaren L, Ploplis B, Shotland LI, Ives E, Riazuddin S, Friedman TB, Morell RJ, Wilcox ER. Characterization of a new full length TMPRSS3 isoform and identification of mutant alleles responsible for nonsyndromic recessive deafness in Newfoundland and Pakistan. BMC Med Genet. 2004;5:24. doi: 10.1186/1471-2350-5-24. [DOI] [PMC free article] [PubMed] [Google Scholar]
  4. Bashir R, Fatima A, Naz S. Mutations in CLDN14 are associated with different hearing thresholds. J Hum Genet. 2010;55:767–770. doi: 10.1038/jhg.2010.104. [DOI] [PMC free article] [PubMed] [Google Scholar]
  5. Bashir ZE, Latief N, Belyantseva IA, Iqbal F, Riazuddin SA, Khan SN, Friedman TB, Riazuddin S, Riazuddin S. Phenotypic variability of CLDN14 mutations causing DFNB29 hearing loss in the Pakistani population. J Hum Genet. 2013;58:102–108. doi: 10.1038/jhg.2012.143. [DOI] [PMC free article] [PubMed] [Google Scholar]
  6. Bear JC, Nemec TF, Kennedy JC, Marshall WH, Power AA, Kolonel VM, Burke GB. Persistent genetic isolation in outport Newfoundland. Am J Med Genet. 1987;27:807–830. doi: 10.1002/ajmg.1320270410. [DOI] [PubMed] [Google Scholar]
  7. Bear JC, Nemec TF, Kennedy JC, Marshall WH, Power AA, Kolonel VM, Burke GB. Inbreeding in outport Newfoundland. Am J Med Genet. 1988;29:649–660. doi: 10.1002/ajmg.1320290324. [DOI] [PubMed] [Google Scholar]
  8. Ben-Yosef T, Belyantseva IA, Saunders TL, Hughes ED, Kawamoto K, Van Itallie CM, Beyer LA, Halsey K, Gardner DJ, Wilcox ER, Rasmussen J, Anderson JM, Dolan DF, Forge A, Raphael Y, Camper SA, Friedman TB. Claudin 14 knockout mice, a model for autosomal recessive deafness DFNB29, are deaf due to cochlear hair cell degeneration. Hum Mol Genet. 2003;12:2049–2061. doi: 10.1093/hmg/ddg210. [DOI] [PubMed] [Google Scholar]
  9. Bespalova IN, Van Camp G, Bom SJ, Brown DJ, Cryns K, DeWan AT, Erson AE, Flothmann K, Kunst HP, Kurnool P, Sivakumaran TA, Cremers CW, Leal SM, Burmeister M, Lesperance MM. Mutations in the Wolfram syndrome 1 gene (WFS1) are a common cause of low frequency sensorineural hearing loss. Hum Mol Genet. 2001;10:2501–2508. doi: 10.1093/hmg/10.22.2501. [DOI] [PMC free article] [PubMed] [Google Scholar]
  10. Charif M, Bakhchane A, Abidi O, Boulouiz R, Eloualid A, Roky R, Rouba H, Kandil M, Lenaers G, Barakat A. Analysis of CLDN14 gene in deaf Moroccan patients with non-syndromic hearing loss. Gene. 2013;523:103–105. doi: 10.1016/j.gene.2013.03.123. [DOI] [PubMed] [Google Scholar]
  11. Chaussenot A, Rouzier C, Quere M, Plutino M, Ait-El-Mkadem S, Bannwarth S, Barth M, Dollfus H, Charles P, Nicolino M, Chabrol B, Vialettes B, Paquis-Flucklinger V. Mutation update and uncommon phenotypes in a French cohort of 96 patients with WFS1-related disorders. Clin Genet. 2015;87:430–439. doi: 10.1111/cge.12437. [DOI] [PubMed] [Google Scholar]
  12. Doucette L, Merner ND, Cooke S, Ives E, Galutira D, Walsh V, Walsh T, MacLaren L, Cater T, Fernandez B, Green JS, Wilcox ER, Shotland LI, Li XC, Lee M, King MC, Young TL. Profound, prelingual nonsyndromic deafness maps to chromosome 10q21 and is caused by a novel missense mutation in the Usher syndrome type IF gene PCDH15. Eur J Hum Genet. 2009;17:554–564. doi: 10.1038/ejhg.2008.231. [DOI] [PMC free article] [PubMed] [Google Scholar]
  13. Ehret G. Stiffness gradient along the basilar membrane as a basis for spatial frequency analysis within the cochlea. J Acoust Soc Am. 1978;64:1723–1726. doi: 10.1121/1.382153. [DOI] [PubMed] [Google Scholar]
  14. Goncalves AC, Matos TD, Simoes-Teixeira HR, Pimenta Machado M, Simao M, Dias OP, Andrea M, Fialho G, Caria H. WFS1 and non-syndromic low-frequency sensorineural hearing loss: a novel mutation in a Portuguese case. Gene. 2014;538:288–291. doi: 10.1016/j.gene.2014.01.040. [DOI] [PubMed] [Google Scholar]
  15. Haywood AF, Merner ND, Hodgkinson KA, Houston J, Syrris P, Booth V, Connors S, Pantazis A, Quarta G, Elliott P, McKenna W, Young TL. Recurrent missense mutations in TMEM43 (ARVD5) due to founder effects cause arrhythmogenic cardiomyopathies in the UK and Canada. Eur Heart J. 2013;34:1002–1011. doi: 10.1093/eurheartj/ehs383. [DOI] [PubMed] [Google Scholar]
  16. Hildebrand MS, DeLuca AP, Taylor KR, Hoskinson DP, Hur IA, Tack D, McMordie SJ, Huygen PL, Casavant TL, Smith RJ. A contemporary review of AudioGene audioprofiling: a machine-based candidate gene prediction tool for autosomal dominant nonsyndromic hearing loss. Laryngoscope. 2009;119:2211–2215. doi: 10.1002/lary.20664. [DOI] [PMC free article] [PubMed] [Google Scholar]
  17. Hodgkinson KA, Howes AJ, Boland P, Shen XS, Stuckless S, Young TL, Curtis F, Collier A, Parfrey PS, Connors SP (2016) Long-Term Clinical Outcome of Arrhythmogenic Right Ventricular Cardiomyopathy in Individuals With a p.S358L Mutation in TMEM43 Following Implantable Cardioverter Defibrillator Therapy. Circ Arrhythm Electrophysiol 9. doi:10.1161/CIRCEP.115.003589 [DOI] [PubMed]
  18. Lee K, Ansar M, Andrade PB, Khan B, Santos-Cortez RL, Ahmad W, Leal SM. Novel CLDN14 mutations in Pakistani families with autosomal recessive non-syndromic hearing loss. Am J Med Genet A. 2012;158A:315–321. doi: 10.1002/ajmg.a.34407. [DOI] [PMC free article] [PubMed] [Google Scholar]
  19. Manion JJ. The Peopleing of Newfoundland: Essays in Historical Geography. St. John’s: Institute of Scoial and Economic Research Memorial University of Newfoundland; 1977. [Google Scholar]
  20. Merner ND, Hodgkinson KA, Haywood AF, Connors S, French VM, Drenckhahn JD, Kupprion C, Ramadanova K, Thierfelder L, McKenna W, Gallagher B, Morris-Larkin L, Bassett AS, Parfrey PS, Young TL (2008) Arrhythmogenic right ventricular cardiomyopathy type 5 is a fully penetrant, lethal arrhythmic disorder caused by a missense mutation in the TMEM43 gene. Am J Hum Genet 82: 809–821. doi:10.1016/j.ajhg.2008.01.010 [DOI] [PMC free article] [PubMed]
  21. Miller SA, Dykes DD, Polesky HF. A simple salting out procedure for extracting DNA from human nucleated cells. Nucleic Acids Res. 1988;16:1215. doi: 10.1093/nar/16.3.1215. [DOI] [PMC free article] [PubMed] [Google Scholar]
  22. Milting H, Klauke B, Christensen AH, Musebeck J, Walhorn V, Grannemann S, Munnich T, Saric T, Rasmussen TB, Jensen HK, Mogensen J, Baecker C, Romaker E, Laser KT, zu Knyphausen E, Kassner A, Gummert J, Judge DP, Connors S, Hodgkinson K, Young TL, van der Zwaag PA, van Tintelen JP, Anselmetti D. The TMEM43 Newfoundland mutation p. S358L causing ARVC-5 was imported from Europe and increases the stiffness of the cell nucleus. Eur Heart J. 2015;36:872–881. doi: 10.1093/eurheartj/ehu077. [DOI] [PubMed] [Google Scholar]
  23. Mineta K, Yamamoto Y, Yamazaki Y, Tanaka H, Tada Y, Saito K, Tamura A, Igarashi M, Endo T, Takeuchi K, Tsukita S. Predicted expansion of the claudin multigene family. FEBS Lett. 2011;585:606–612. doi: 10.1016/j.febslet.2011.01.028. [DOI] [PubMed] [Google Scholar]
  24. Morton CC, Nance WE (2006) Newborn hearing screening - silent revolution. N Engl J Med 354:2151в164. doi:10.1056/NEJMra050700 [DOI] [PubMed]
  25. Nayak G, Varga L, Trincot C, Shahzad M, Friedman PL, Klimes I, Greinwald JH, Riazuddin SA, Masindova I, Profant M, Khan SN, Friedman TB, Ahmed ZM, Gasperikova D, Riazuddin S, Riazuddin S. Molecular genetics of MARVELD2 and clinical phenotype in Pakistani and Slovak families segregating DFNB49 hearing loss. Hum Genet. 2015;134(4):423–437. doi: 10.1007/s00439-015-1532-y. [DOI] [PMC free article] [PubMed] [Google Scholar]
  26. Purcell SM, Moran JL, Fromer M, Ruderfer D, Solovieff N, Roussos P, O’Dushlaine C, Chambert K, Bergen SE, Kahler A, Duncan L, Stahl E, Genovese G, Fernandez E, Collins MO, Komiyama NH, Choudhary JS, Magnusson PK, Banks E, Shakir K, Garimella K, Fennell T, DePristo M, Grant SG, Haggarty SJ, Gabriel S, Scolnick EM, Lander ES, Hultman CM, Sullivan PF, McCarroll SA, Sklar P (2014) A polygenic burden of rare disruptive mutations in schizophrenia. Nature 506:185–190. doi:10.1038/nature12975 [DOI] [PMC free article] [PubMed]
  27. Riazuddin S, Ahmed ZM, Fanning AS, Lagziel A, Kitajiri S, Ramzan K, Khan SN, Chattaraj P, Friedman PL, Anderson JM, Belyantseva IA, Forge A, Riazuddin S, Friedman TB (2006) Tricellulin is a tight-junction protein necessary for hearing. Am J Hum Genet 79: 1040–1051. doi:10.1086/510022 [DOI] [PMC free article] [PubMed]
  28. Richards S, Aziz N, Bale S, Bick D, Das S, Gastier-Foster J, Grody WW, Hegde M, Lyon E, Spector E, Voelkerding K, Rehm HL, Committee ALQA. Standards and guidelines for the interpretation of sequence variants: a joint consensus recommendation of the American College of Medical Genetics and Genomics and the Association for Molecular Pathology. Genet Med. 2015;17:405–424. doi: 10.1038/gim.2015.30. [DOI] [PMC free article] [PubMed] [Google Scholar]
  29. Scheffer DI, Shen J, Corey DP, Chen ZY (2015) Gene Expression by Mouse Inner Ear Hair Cells during Development J Neurosci 35:6366–6380. doi:10.1523/JNEUROSCI.5126-14.2015 [DOI] [PMC free article] [PubMed]
  30. Seary ER (1977) Family Names of the Island of Newfoundland. McGill-Queen’s University Press, St. John’s
  31. Sloan-Heggen CM, Babanejad M, Beheshtian M, Simpson AC, Booth KT, Ardalani F, Frees KL, Mohseni M, Mozafari R, Mehrjoo Z, Jamali L, Vaziri S, Akhtarkhavari T, Bazazzadegan N, Nikzat N, Arzhangi S, Sabbagh F, Otukesh H, Seifati SM, Khodaei H, Taghdiri M, Meyer NC, Daneshi A, Farhadi M, Kahrizi K, Smith RJ, Azaiez H, Najmabadi H (2015) Characterising the spectrum of autosomal recessive hereditary hearing loss in Iran. J Med Genet 52:823–829. doi:10.1136/jmedgenet-2015-103389 [DOI] [PMC free article] [PubMed]
  32. Sloan-Heggen CM, Bierer AO, Shearer AE, Kolbe DL, Nishimura CJ, Frees KL, Ephraim SS, Shibata SB, Booth KT, Campbell CA, Ranum PT, Weaver AE, Black-Ziegelbein EA, Wang D, Azaiez H, Smith RJ (2016) Comprehensive genetic testing in the clinical evaluation of 1119 patients with hearing loss. Hum Genet 135: 441-50. doi:10.1007/s00439-016-1648-8 [DOI] [PMC free article] [PubMed]
  33. Smith RJH, Shearer AE, Hildebrand MS, et al. Deafness and Hereditary Hearing Loss Overview. 1999 Feb 14 [Updated 2014 Jan 9]. In: Pagon RA, Adam MP, Ardinger HH, et al., editors. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 1993-2016. Available from: http://www.ncbi.nlm.nih.gov/books/NBK1434/. Accessed May 21 2016
  34. Sun Y, Cheng J, Lu Y, Li J, Lu Y, Jin Z, Dai P, Wang R, Yuan H. Identification of two novel missense WFS1 mutations, H696Y and R703H, in patients with non-syndromic low-frequency sensorineural hearing loss. J Genet Genomics. 2011;38:71–76. doi: 10.1016/j.jcg.2011.01.001. [DOI] [PubMed] [Google Scholar]
  35. Teudt IU, Richter CP. Basilar membrane and tectorial membrane stiffness in the CBA/CaJ mouse. J Assoc Res Otolaryngol. 2014;15:675–694. doi: 10.1007/s10162-014-0463-y. [DOI] [PMC free article] [PubMed] [Google Scholar]
  36. Thorleifsson G, Holm H, Edvardsson V, Walters GB, Styrkarsdottir U, Gudbjartsson DF, Sulem P, Halldorsson BV, de Vegt F, d’Ancona FC, den Heijer M, Franzson L, Christiansen C, Alexandersen P, Rafnar T, Kristjansson K, Sigurdsson G, Kiemeney LA, Bodvarsson M, Indridason OS, Palsson R, Kong A, Thorsteinsdottir U, Stefansson K. Sequence variants in the CLDN14 gene associate with kidney stones and bone mineral density. Nat Genet. 2009;41:926–930. doi: 10.1038/ng.404. [DOI] [PubMed] [Google Scholar]
  37. Toka HR, Genovese G, Mount DB, Pollak MR, Curhan GC (2013) Frequency of rare allelic variation in candidate genes among individuals with low and high urinary calcium excretion. PLoS One 8:e71885. doi:10.1371/journal.pone.0071885 [DOI] [PMC free article] [PubMed]
  38. Untergasser A, Cutcutache I, Koressaar T, Ye J, Faircloth BC, Remm M and Rozen SG (2012) Primer3–new capabilities and interfaces. Nucleic Acids Res 40(15):e115 [DOI] [PMC free article] [PubMed]
  39. Van Camp G, Smith RJH (2015) Hereditary Hearing Loss Homepage. http://hereditaryhearingloss.org/. Accessed May 21, 2016
  40. Wattenhofer M, Reymond A, Falciola V, Charollais A, Caille D, Borel C, Lyle R, Estivill X, Petersen MB, Meda P, Antonarakis SE. Different mechanisms preclude mutant CLDN14 proteins from forming tight junctions in vitro. Hum Mutat. 2005;25:543–549. doi: 10.1002/humu.20172. [DOI] [PubMed] [Google Scholar]
  41. Wilcox ER, Burton QL, Naz S, Riazuddin S, Smith TN, Ploplis B, Belyantseva I, Ben-Yosef T, Liburd NA, Morell RJ, Kachar B, Wu DK, Griffith AJ, Riazuddin S, Friedman TB. Mutations in the gene encoding tight junction claudin-14 cause autosomal recessive deafness DFNB29. Cell. 2001;104:165–172. doi: 10.1016/S0092-8674(01)00200-8. [DOI] [PubMed] [Google Scholar]
  42. Yan D, Tekin D, Bademci G, Foster J, Cengiz FB, Kannan-Sundhari A, Guo S, Mittal R, Zou B, Grati M, Kabahuma RI, Kameswaran M, Lasisi TJ, Adedeji WA, Lasisi AO, Menendez I, Herrera M, Carranza C, Maroofian R, Crosby AH, Bensaid M, Masmoudi S, Behnam M, Mojarrad M, Feng Y, Duman D, Mawla AM, Nord AS, Blanton SH, Liu XZ, Tekin M. Spectrum of DNA variants for non-syndromic deafness in a large cohort from multiple continents. Hum Genet. 2016;135(8):953–961. doi: 10.1007/s00439-016-1697-z. [DOI] [PMC free article] [PubMed] [Google Scholar]
  43. Young TL, Ives E, Lynch E, Person R, Snook S, MacLaren L, Cater T, Griffin A, Fernandez B, Lee MK, King MC. Non-syndromic progressive hearing loss DFNA38 is caused by heterozygous missense mutation in the Wolfram syndrome gene WFS1. Hum Mol Genet. 2001;10:2509–2514. doi: 10.1093/hmg/10.22.2509. [DOI] [PubMed] [Google Scholar]
  44. Zhai G, Zhou J, Woods MO, Green JS, Parfrey P, Rahman P, Green RC. Genetic structure of the Newfoundland and Labrador population: founder effects modulate variability. Eur J Hum Genet. 2015 doi: 10.1038/ejhg.2015.256. [DOI] [PMC free article] [PubMed] [Google Scholar]

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