← Evidence map

ArticleJapanese journal of ophthalmology

Mutation c. 1142 del G in the PRPF31 gene in a family with autosomal dominant retinitis pigmentosa (RP11) and its implications.

Kurenai Taira et al.PubMed ↗Publisher ↗

No numbers read from the abstract.

8 papers cite it

2008
2009
2010
2011
2012
2013
2014
2015
2016
2017
2018
2019
2020
trialcites it
Full record →Abstract, authors, funding and every citing paper · PMID 17295140