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Article

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

Molecular vision - 1 Mar 2007

Zhang Qingjiong, Xiao Xueshan, Li Shiqiang, Jia Xiaoyun, Yang Zhikuan, Huang Shizhou, Caruso Rafael C, Guan Tianqin, Sergeev Yuri, Guo Xiangming, Hejtmancik J Fielding

Abstract excerpt

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 night blindness (CSNB1). High myopia is usually observed in patients with CSNB1. This study was designed to test the...

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Identifiers

PMID: 17392683
PMCID: PMC2642916

Genes

NYX

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-07.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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Mutations in NYX of individuals with high myopia, but without night blindness.PMID 17392683Read ↗

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