Genetic and clinical landscape of ARR3-associated MYP26: the most common cause of Mendelian early-onset high myopia with a unique inheritance

AIMS: To elucidate genetic background of early-onset high myopia (eoHM) and characteristics of ARR3-associated MYP26. METHODS: Variants in 14 genes reported to contribute to eoHM, including ARR3, were selected from exome sequencing data set and classified into different categories following American...

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Detalles Bibliográficos
Autores principales: Wang, Yingwei, Xiao, Xueshan, Li, Xueqing, Yi, Zhen, Jiang, Yi, Zhang, Fengsheng, Zhou, Lin, Li, Shiqiang, Jia, Xiaoyun, Sun, Wenmin, Wang, Panfeng, Zhang, Qingjiong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BMJ Publishing Group 2023
Materias:
Clinical Science
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10579186/
https://www.ncbi.nlm.nih.gov/pubmed/36180177
http://dx.doi.org/10.1136/bjo-2022-321511

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10579186/
https://www.ncbi.nlm.nih.gov/pubmed/36180177
http://dx.doi.org/10.1136/bjo-2022-321511

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