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. 2013 Nov 18;8(11):e79063. doi: 10.1371/journal.pone.0079063

Figure 1. A large Korean family with autosomal dominant late-onset nonsyndromic hearing loss.

Figure 1

(A) The pedigree with the proband (IV-20) indicated by an arrow. Individuals who participated in the molecular genetic diagnosis are marked with an asterisk on the right shoulder of symbols. Whole exome sequencing was performed in 4 individuals (IV:3, IV:17, V:1 and V:5). The genotypes at theArg326Lys mutation site of POU4F3are presented for each individual (mutant allele “A” in red). (B) Audiograms of 4 affected individuals in the family including the proband.