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Pedigree and haplotypes (family DDL4), co-segregating nonsyndromic autosomal recessive hearing loss (filled symbols) with short tandem repeat markers at the DFNB7/11 locus. Sequence chromatogram of transmembrane channel like 1 gene showing homozygous change c.100C>T (p.R34X) in hearing impaired children, parents and normal hearing child are heterozygous for c.100C>T.
