Novel mutation in the γ-S crystallin gene causing autosomal dominant cataract

PURPOSE: To identify the underlying genetic defect in a north Indian family with seven members in three-generations affected with bilateral congenital cataract. METHODS: Detailed family history and clinical data were recorded. Linkage analysis using fluorescently labeled microsatellite markers for t...

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Detalles Bibliográficos
Autores principales: Vanita, Vanita, Singh, Jai Rup, Singh, Daljit, Varon, Raymonda, Sperling, Karl
Formato: Texto
Lenguaje:English
Publicado: Molecular Vision 2009
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2650718/
https://www.ncbi.nlm.nih.gov/pubmed/19262743

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2650718/
https://www.ncbi.nlm.nih.gov/pubmed/19262743

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