RPE65 and Leber congenital amaurosis 2: Specifically, we used the Pde6βRd10 (rd10) and RhoP23H/WT (P23H) mouse models of autosomal recessive and autosomal dominant RP, respectively, as well as the Rpe65−/− mouse model of Leber’s congenital amaurosis type 2 (LCA2).