Mutations in NYX of individuals with high myopia, but without night blindness

PURPOSE: High myopia is a common genetic variant that severely affects vision. Genes responsible for myopia without linked additional functional defects have not been identified. Mutations in the nyctalopin gene (NYX) located at Xp11.4 are responsible for a complete form of congenital stationary nig...

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Detalles Bibliográficos
Autores principales: Zhang, Qingjiong, Xiao, Xueshan, Li, Shiqiang, Jia, Xiaoyun, Yang, Zhikuan, Huang, Shizhou, Caruso, Rafael C., Guan, Tianqin, Sergeev, Yuri, Guo, Xiangming, Hejtmancik, J. Fielding
Formato: Texto
Lenguaje:English
Publicado: Molecular Vision 2007
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2642916/
https://www.ncbi.nlm.nih.gov/pubmed/17392683

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2642916/
https://www.ncbi.nlm.nih.gov/pubmed/17392683

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