Article
NYX mutations in four families with high myopia with or without CSNB1.
Molecular vision - 1 Jan 2015
Zhou Lin, Li Tuo, Song Xiusheng, Li Yin, Li Hongyan, Dan Handong
Abstract excerpt
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 having high myopia with or without CSNB1 and 96 normal controls were recruited. We searched for mutations in the...
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