Clinical and genetic findings of a Japanese patient with RP1 -related autosomal recessive retinitis pigmentosa

ConclusionThis is the first description of a Japanese patient with arRP caused byRP1 mutations. Additional data are necessary to more accurately determine the clinical course and mutation spectrum in patients withRP1-related arRP.

Source: Documenta Ophthalmologica - July 19, 2018 Category: Opthalmology Source Type: research