Clinical characterization of autosomal dominant retinitis pigmentosa with NRL mutation in a three-generation Japanese family.
Kei MizobuchiTakaaki HayashiTomokazu MatsuuraTadashi NakanoPublished in: Documenta ophthalmologica. Advances in ophthalmology (2022)
Our results indicated that retinal construction and function were aggravated in an age-dependent manner, and retinal degeneration, especially in the macular region, revealed milder findings than in previous cases with NRL-associated AD-RP.