Two novel mutations in the bestrophin-1 gene and associated clinical observations in patients with best vitelliform macular dystrophy-Reference-Cited by-同舟云学术

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Two novel mutations in the bestrophin-1 gene and associated clinical observations in patients with best vitelliform macular dystrophy

Published:2015-04-30 Issue:2 Volume:12 Page:2584-2588
ISSN:1791-2997
Container-title:Molecular Medicine Reports
language:en
Short-container-title:

Author:

LIN YING,GAO HONGBIN,LIU YUHUA,LIANG XUANWEI,LIU XIALIN,WANG ZHONGHAO,ZHANG WANJUN,CHEN JIANGNA,LIN ZHUOLING,HUANG XINHUA,LIU YIZHI

Publisher

Spandidos Publications

Subject

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

Cited by 9 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. Vitelliform Macular Dystrophy;Inherited Retinal Disease;2022

2. A novel mutation of BEST1 gene in Best disease;European Journal of Ophthalmology;2020-04-22

3. “Novel p.Tyr284Cys BEST1 genotype–phenotype correlations of Vitelliform Macular Dystrophy in a family with incomplete penetrance”;Ophthalmic Genetics;2020-03-03

4. Clinical Genetics of Vitelliform Macular Dystrophy: An Asian Perspective;Essentials in Ophthalmology;2018-11-04

5. An allosteric mechanism of inactivation in the calcium-dependent chloride channel BEST1;Journal of General Physiology;2018-09-20

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