A novel splicing mutation in the PRPH2 gene causes autosomal dominant retinitis pigmentosa in a Chinese pedigree.

A novel splicing mutation in the PRPH2 gene causes autosomal dominant retinitis pigmentosa in a Chinese pedigree.
J Cell Mol Med. 2019 Mar 20;:
Authors: Cheng J, Fu J, Zhou Q, Xiang X, Wei C, Yang L, Fu S, Khan MA, Lv H, Fu J
PMID: 30892800 [PubMed - as supplied by publisher]

Source: J Cell Mol Med - March 19, 2019 Category: Molecular Biology Authors: Cheng J, Fu J, Zhou Q, Xiang X, Wei C, Yang L, Fu S, Khan MA, Lv H, Fu J Tags: J Cell Mol Med Source Type: research