Figure 2From: A novel missense mutation in the CLCN7 gene linked to benign autosomal dominant osteopetrosis: a case series Electropherogram results of CLCN7 exon 15 sequencing derived from a family with a history of autosomal dominant osteopetrosis-II and a control individual. The c.1225C>T position is indicated. Codon C GG is changed to T GG (p.Arg409Trp).Back to article page