Fig. 3From: Exome sequencing identifies a mutation in TMC1 as a novel cause of autosomal recessive nonsyndromic hearing lossMutation analysis of the Chinese family SH-02. a DNA sequences of homozygous missense c.1979C>T mutations and the wild-type control. b The structure of TMC1A depicts the position of c.1979C>T, a mutation in exon 20 and p.P660L in TM2 domainBack to article page