← Evidence map

ArticleInvestigative ophthalmology & visual science2013

Mutations in the X-linked retinitis pigmentosa genes RPGR and RP2 found in 8.5% of families with a provisional diagnosis of autosomal dominant retinitis pigmentosa.

Jennifer D Churchill et al.PubMed ↗Full text ↗Publisher ↗

No numbers read from the abstract.

82 papers cite itlatest 60 shown

2013
…
2014
2015
2016
2017
2018
2019
2020
2021
2022
2023
2024
2026
this papertrialcites it
Full record →Abstract, authors, funding and every citing paper · PMID 23372056