Fig. 5From: Consanguinity-based analysis of exome sequencing yields likely genetic causes in patients with inherited retinal dystrophyProportion of correlated phenotypes of mutated RDH12 and CRB1. Pie charts illustrate the proportion of heterogeneous phenotypes correlated with RDH12 mutations (A) and CRB1 mutations (B). ARRP: autosomal recessive retinitis pigmentosa. ADRP: autosomal dominant retinitis pigmentosa. ARLCA: autosomal recessive Leber congenital amaurosis. CORD: cone and rod dystrophy. PPRPE: preserved para-arteriole retinal pigment epithelium. FFR: familial foveal retinoschisisBack to article page