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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 famil...

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Source

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Identifiers

PMID: 25802485
PMCID: PMC4357032

Genes

NYX

Variants

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 4 Sept 2026. Prepared record publication-25802485-2026-09-04.2. Manifest publication-graph-cohort-2026-09-04.2.

Source receipt: PubMed via Helena Literature Corpus, retrieved 4 Sept 2026.

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