Unique Haplotypes in <i>OPN1LW</i> as a Common Cause of High Myopia With or Without Protanopia: A Potential Window Into Myopic Mechanism-Reference-Cited by-同舟云学术

Unique Haplotypes in OPN1LW as a Common Cause of High Myopia With or Without Protanopia: A Potential Window Into Myopic Mechanism

Published:2023-04-25 Issue:4 Volume:64 Page:29
ISSN:1552-5783
Container-title:Investigative Opthalmology & Visual Science
language:en
Short-container-title:Invest. Ophthalmol. Vis. Sci.

Author:

Wang Yingwei¹,Sun Wenmin¹,Xiao Xueshan¹,Jiang Yi¹,Ouyang Jiamin¹,Wang Junwen¹,Yi Zhen¹,Li Shiqiang¹,Jia Xiaoyun¹,Wang Panfeng¹,Hejtmancik J. Fielding²,Zhang Qingjiong¹

Affiliation:

1. State Key Laboratory of Ophthalmology, Zhongshan Ophthalmic Center, Sun Yat-sen University, Guangdong Provincial Key Laboratory of Ophthalmology and Visual Science, Guangzhou, China

2. Ophthalmic Molecular Genetics Section, Ophthalmic Genetics and Visual Function Branch, National Eye Institute, Rockville, Maryland, United States

Publisher

Association for Research in Vision and Ophthalmology (ARVO)

Subject

General Medicine

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