NDLI: Novel compound heterozygous mutation in the CNGA1 gene underlie autosomal recessive retinitis pigmentosa in a Chinese family.

Content Provider	Europe PMC
Author	Jin, Xin Qu, Ling-Hui Hou, Bao-Ke Xu, Hai-Wei Meng, Xiao-Hong Pang, Chi-Pui Yin, Zheng-Qin
Copyright Year	2016
Page Count	8
ISSN	01448463
Volume Number	36
PubMed Central reference number	PMC4725244
Issue Number	1
PubMed reference number	26802146
Journal	Bioscience Reports [Biosci. Rep]
e-ISSN	15734935
DOI	10.1042/BSR20150131
Language	English
Publisher	Portland Press Ltd.
Publisher Date	2016-01-22
Access Restriction	Open
Rights License	This is an open access article published by Portland Press Limited and distributed under the Creative Commons Attribution Licence 3.0. © 2016 Authors
Subject Keyword	CNGA1 mutation next-generation sequencing retinitis pigmentosa
Content Type	Text
Resource Type	Article
Subject	Cell Biology Molecular Biology Biochemistry Biophysics

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