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

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....

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Detalles Bibliográficos
Autores principales: Gu, Yonghao, Wang, Lifeng, Zhou, Jie, Guo, Qun, Liu, Na, Ding, Zhenqiang, Li, Li, Liu, Xinping, An, Jing, Yan, Guolin, Yao, Libo, Zhang, Zuoming
Formato: Texto
Lenguaje:English
Publicado: Molecular Vision 2008
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2267729/
https://www.ncbi.nlm.nih.gov/pubmed/18246026

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2267729/
https://www.ncbi.nlm.nih.gov/pubmed/18246026

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