GLRA2 gene mutations cause high myopia in humans and mice

BACKGROUND: High myopia (HM) is a leading cause of blindness that has a strong genetic predisposition. However, its genetic and pathogenic mechanisms remain largely unknown. Thus, this study aims to determine the genetic profile of individuals from two large Chinese families with HM and 200 patients...

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Detalles Bibliográficos
Autores principales: Tian, Qi, Tong, Ping, Chen, Gong, Deng, Meichun, Cai, Tian'e, Tian, Runyi, Zhang, Zimin, Xia, Kun, Hu, Zhengmao
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BMJ Publishing Group 2023
Materias:
Novel Disease Loci
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9887403/
https://www.ncbi.nlm.nih.gov/pubmed/35396272
http://dx.doi.org/10.1136/jmedgenet-2022-108425

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9887403/
https://www.ncbi.nlm.nih.gov/pubmed/35396272
http://dx.doi.org/10.1136/jmedgenet-2022-108425

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