Bestrophin 1 gene analysis and associated clinical findings in a Chinese patient with Best vitelliform macular dystrophy-Reference-Cited by-同舟云学术

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Bestrophin 1 gene analysis and associated clinical findings in a Chinese patient with Best vitelliform macular dystrophy

Published:2017-08-04 Issue:4 Volume:16 Page:4751-4755
ISSN:1791-2997
Container-title:Molecular Medicine Reports
language:en
Short-container-title:

Author:

Lin Ying,Li Tao,Gao Hongbin,Lian Yu,Chen Chuan,Zhu Yi,Li Yonghao,Liu Bingqian,Zhou Wenli,Jiang Hongye,Liu Xialin,Zhao Xiujuan,Liang Xiaoling,Jin Chenjin,Huang Xinhua,Lu Lin

Publisher

Spandidos Publications

Subject

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

Cited by 10 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. First Pediatric Case of Autosomal Recessive Homozygotic Bestrophinopathy due to Homozygous Mutation c.187G>C p. in Two Brothers;Journal of Clinical Medicine Research;2022-04

2. Novel mutations in the BEST1 gene cause distinct retinopathies in two Chinese families;International Journal of Ophthalmology;2022-02-18

3. Vitelliform Macular Dystrophy;Inherited Retinal Disease;2022

4. Multimodal imaging and genetic analysis of adult‑onset best vitelliform macular dystrophy in Chinese patients;Experimental and Therapeutic Medicine;2021-07-19

5. A Case of Best Disease Accompanied by Pachychoroid Neovasculopathy;Turkish Journal of Ophthalmology;2019-08-01

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