Case Report: A Novel Mutation in the CRYGD Gene Causing Congenital Cataract Associated with Nystagmus in a Chinese Family

Purpose: Congenital cataract (CC) is a common disease resulting in leukocoria and the leading cause of blindness in children worldwide. Approximately 50% of congenital cataract is inherited. Our aim is to identify mutations in a Chinese family with congenital cataract. Methods: A four-generation Chi...

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Detalles Bibliográficos
Autores principales: Gao, Yunxia, Ren, Xiang, Fu, Xiangyu, Lin, Yu, Xiao, Lirong, Wang, Xiaoyue, Yan, Naihong, Zhang, Ming
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Genetics
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8866695/
https://www.ncbi.nlm.nih.gov/pubmed/35222542
http://dx.doi.org/10.3389/fgene.2022.824550

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8866695/
https://www.ncbi.nlm.nih.gov/pubmed/35222542
http://dx.doi.org/10.3389/fgene.2022.824550

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