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Article

A naturally-occurring mutation in Cacna1f in a rat model of congenital stationary night blindness.

Molecular vision - 9 Jan 2008

Gu Yonghao, Wang Lifeng, Zhou Jie, Guo Qun, Liu Na, Ding Zhenqiang, Li Li, Liu Xinping, An Jing, Yan Guolin, Yao Libo, Zhang Zuoming

Abstract excerpt

PURPOSE: To identify the gene mutation responsible for a previously described rat model of X-linked congenital stationary night blindness (CSNB). METHODS: Rat orthologous genes for Nyx and Cacna1f were isolated from retina through rapid amplification the cDNA ends (RACE) and examined for mutations. Electroretinograms were used to identify affected animals. RESULTS: The rat Nyx cDNA spans 1,971 nucleotides and...

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Identifiers

PMID: 18246026
PMCID: PMC2267729

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ERG

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

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