NR2E3 and retinitis pigmentosa 1: Mutations on the NR2E3 gene have been described with an autosomal dominant form of RP (NR2E3, OMIM #604485: autosomal dominant) showing a phenotype similar to classic RP with initial impairment of the rods and subsequent involvement of the cones, and the presence in fundus photography of bone spiculae in the midperiphery [61].