Targeted Next Generation Sequencing Identifies Novel Mutations in RP1 as a Relatively Common Cause of Autosomal Recessive Rod-Cone Dystrophy

Figure 3

Pedigrees of seven families with RP1 mutations underlying autosomal recessive rod-cone dystrophy. Affected and unaffected individuals are represented by shapes filled with black and white colors, respectively. Men and women are indicated by squares and circles, respectively. Index subjects are marked by . Consanguinity is marked by a double horizontal line.