Fig. 3From: Novel compound heterozygous mutations in CNGA1in a Chinese family affected with autosomal recessive retinitis pigmentosa by targeted sequencingCNGA1 sequence variation analysis. CNGA1 sequence variation pattern are clarified into three types: wild type, no mutation in the two loci; carrier, only one of the two loci in mutant status; affected: two loci were in mutant status. Individuals belong to each type are presented in parenthesisBack to article page