NYX mutations in four families with high myopia with or without CSNB1

PURPOSE: Mutations in the NYX gene are known to cause complete congenital stationary night blindness (CSNB1), which is always accompanied by high myopia. In this study, we aimed to investigate the association between NYX mutations and high myopia with or without CSNB1. METHODS: Four Chinese families...

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Detalles Bibliográficos
Autores principales: Zhou, Lin, Li, Tuo, Song, Xiusheng, Li, Yin, Li, Hongyan, Dan, Handong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Molecular Vision 2015
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4357032/
https://www.ncbi.nlm.nih.gov/pubmed/25802485

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4357032/
https://www.ncbi.nlm.nih.gov/pubmed/25802485

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