Fig. 2From: Next-generation sequencing for D47N mutation in Cx50 analysis associated with autosomal dominant congenital cataract in a six-generation Chinese familyThe mutation in Cx50 was confirmed with Sanger sequencing. a a heterozygous mutation c.139 G > A was identified in all affected participants. b Sequence of unaffected individual. c Sequence of control. The amino acid reading-frame is indicated, GAT encodes Asp (D), and AAT encodes Asn (N)Back to article page