The Genetic Confirmation and Clinical Characterization of LOXL3-Associated MYP28: A Common Type of Recessive Extreme High Myopia

Author:

Jiang Yi1,Zhou Lin2,Wang Yingwei1,Ouyang Jiamin1,Li Shiqiang1,Xiao Xueshan1,Jia Xiaoyun1,Wang Junwen1,Yi Zhen1,Sun Wenmin1,Jiao Xiaodong3,Wang Panfeng1,Hejtmancik J. Fielding3,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. Department of Ophthalmology, West China Hospital, Sichuan University, Chengdu, China

3. 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

Reference56 articles.

1. IMI - defining and classifying myopia: A proposed set of standards for clinical and epidemiologic studies;Flitcroft;Invest Ophthalmol Vis Sci,2019

2. Genetic susceptibility and mechanisms for refractive error;Stambolian;Clin Genet,2013

3. Myopia;Baird;Nat Rev Dis Primers,2020

4. Insight into the molecular genetics of myopia;Li;Mol Vis,2017

5. Genetic and clinical landscape of ARR3-associated MYP26: The most common cause of Mendelian early-onset high myopia with a unique inheritance [published online ahead of print September 30, 2022];Wang;Br J Ophthalmol

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