Next generation sequencing identified novel heterozygous nonsense mutation in CNGB1 gene associated with retinitis pigmentosa in a Chinese patient-Reference-Cited by-同舟云学术

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Next generation sequencing identified novel heterozygous nonsense mutation in CNGB1 gene associated with retinitis pigmentosa in a Chinese patient

Published:2017-10-10 Issue:51 Volume:8 Page:88345-88350
ISSN:1949-2553
Container-title:Oncotarget
language:en
Short-container-title:Oncotarget

Author:

Banerjee Santasree¹,Yao Junping²,Zhang Xinxin¹,Niu Jianjun³,Chen Zhongshan⁴

Affiliation:

1. Department of Cell Biology and Medical Genetics, School of Medicine, Zhejiang University, Hangzhou, China

2. Department of Ophthalmology, Tianyou Hospital Affiliated to Wuhan University of Science & Technology, Wuhan, China

3. Department of Ophthalmology, General Hospital of Xinjiang Military Area Command of Chinese PLA, Urumqi, China

4. Department of Ophthalmology, Zhongnan Hospital of Wuhan University, Wuhan, China

Publisher

Impact Journals, LLC

Subject

Oncology

Cited by 2 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. CNGB1 ‐related rod‐cone dystrophy: A mutation review and update;Human Mutation;2021-05-16

2. Targeted next-generation sequencing-based molecular diagnosis of congenital hand malformations in Chinese population;Scientific Reports;2018-08-24

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