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A schematic of the distribution of causal mutations reported in RP1 responsible for RP. The red and green bars indicate parts of RP1 where mutations responsible for autosomal dominant retinitis pigmentosa (RP) and autosomal recessive RP, respectively, have been identified. Asterisks are the mutations identified in this study. Note: The deletion identified in PKRP358 removes all three coding exons of RP1.
