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Proportion 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 retinoschisis
