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Sequence variations of GRM6 in patients with high myopia

PURPOSE: Mutations in the glutamate receptor metabotropic 6 gene (GRM6) have been identified in patients with congenital stationary night blindness (CSNB1B). High myopia is usually observed in CSNB1B patients. This study tested if any mutations in GRM6 were solely responsible for high myopia. METHOD...

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Detalles Bibliográficos
Autores principales:	Xu, Xiaoyu, Li, Shiqiang, Xiao, Xueshan, Wang, Panfeng, Guo, Xiangming, Zhang, Qingjiong
Formato:	Texto
Lenguaje:	English
Publicado:	Molecular Vision 2009
Materias:	Research Article
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2765235/ https://www.ncbi.nlm.nih.gov/pubmed/19862333

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