A novel mutation in the MIP gene is associated with autosomal dominant congenital nuclear cataract in a Chinese family

PURPOSE: Congenital cataracts are a clinically and genetically heterogeneous lens disorder. The purpose of this study was to identify the genetic mutation and the molecular phenotype responsible for the presence of autosomal dominant congenital nuclear cataract disease in a Chinese family. METHODS:...

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Detalles Bibliográficos
Autores principales: Yang, Guoxing, Zhang, Guisen, Wu, Qiang, Zhao, Jialiang
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Molecular Vision 2011
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3107997/
https://www.ncbi.nlm.nih.gov/pubmed/21647270

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3107997/
https://www.ncbi.nlm.nih.gov/pubmed/21647270

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