Figure 4From: Development and application of a next-generation-sequencing (NGS) approach to detect known and novel gene defects underlying retinal diseasesDetection of novel mutations using NGS in 254 retinal genes. Novel mutations in PRPF8, CRB1, RPGR and CACNA1F co-segregated in affected and asymptomatic carriers with the adRP, arRP, x-linked dominant and X-liked icCSNB phenotypes respectively. Asymptomatic individuals are marked with a question mark.Back to article page