Identification of CRB1 mutations in two Chinese consanguineous families exhibiting autosomal recessive retinitis pigmentosa-Reference-Cited by-同舟云学术

Identification of CRB1 mutations in two Chinese consanguineous families exhibiting autosomal recessive retinitis pigmentosa

Published:2019-07-12 Issue: Volume: Page:
ISSN:1791-2997
Container-title:Molecular Medicine Reports
language:
Short-container-title:Mol Med Report

Author:

Guo Xiaoxin¹,Li Jie²,Wang Qingwei¹,Shu Yi¹,Wang Jin¹,Chen Lijia³,Zhang Houbin¹,Shi Yi¹,Yang Jiyun¹,Lu Fang¹,Jiang Li¹,Qu Chao²,Gong Bo¹

Affiliation:

1. Key Laboratory for Human Disease Gene Study of Sichuan Province and Department of Laboratory Medicine, Sichuan Academy of Medical Sciences and Sichuan Provincial People's Hospital, School of Medicine, University of Electronic Science and Technology of China, Chengdu, Sichuan 610072, P.R. China

2. Department of Ophthalmology, Sichuan Academy of Medical Sciences and Sichuan Provincial People's Hospital, School of Medicine, University of Electronic Science and Technology of China, Chengdu, Sichuan 610072, P.R. China

3. Department of Ophthalmology and Visual Sciences, The Chinese University of Hong Kong, Hong Kong, SAR, P.R. China

Publisher

Spandidos Publications

Subject

Cancer Research,Oncology,Genetics,Molecular Biology,Molecular Medicine,Biochemistry

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