Identification of two novel RHO mutations in Chinese retinitis pigmentosa patients-Reference-Cited by-同舟云学术

Identification of two novel RHO mutations in Chinese retinitis pigmentosa patients

Published:2019-11 Issue: Volume:188 Page:107726
ISSN:0014-4835
Container-title:Experimental Eye Research
language:en
Short-container-title:Experimental Eye Research

Author:

Wang Juan,Xu Ding,Zhu Tong,Zhou Yue,Chen Xin,Wang Fang,Zhang Jieping,Tian Haibin,Gao Furong,Zhang Jingfa,Jin Caixia,Xu Jingying,Lu Lixia,Liu Qin,Xu Guo-Tong

Funder

National Key Basic Research Program of China

Foundation Fighting Blindness

National Natural Science Foundation of China

Shanghai Municipal Commission of Health and Family Planning

Shanghai Science and Technology Committee

Natural Science Foundation of Shanghai

State Key Laboratory of Ophthalmology

Shanghai East Hospital

Tongji University

Publisher

Elsevier BV

Subject

Cellular and Molecular Neuroscience,Sensory Systems,Ophthalmology

Reference40 articles.

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3. Mutations in the TOPORS gene cause 1% of autosomal dominant retinitis pigmentosa;Bowne;Mol. Vis.,2008

4. Prevalence and causes of visual impairment and blindness among 9980 Scandinavian adults: the Copenhagen City Eye Study;Buch;Ophthalmology,2004

5. Molecular analysis and genetic mapping of the rhodopsin gene in families with autosomal dominant retinitis pigmentosa;Bunge;Genomics,1993

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1. Clinical and genetic features of Koreans with retinitis pigmentosa associated with mutations in rhodopsin;Frontiers in Genetics;2023-08-29

2. Genetic dissection of non-syndromic retinitis pigmentosa;Indian Journal of Ophthalmology;2022

3. Identification of a novel RHO heterozygous nonsense mutation in a Chinese family with autosomal dominant retinitis pigmentosa;BMC Ophthalmology;2021-10-11

4. Retinal Dystrophies and the Road to Treatment: Clinical Requirements and Considerations;Asia-Pacific Journal of Ophthalmology;2020-05