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A novel human CRYGD mutation in a juvenile autosomal dominant cataract

PURPOSE: Identification of causal mutation in the crystallin, connexin, and paired box gene 6 (PAX6) genes associated with childhood cataract in patients from India. METHODS: In this study, forty eight members from seventeen families and 148 sporadic cases of childhood cataract were evaluated. Clini...

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Detalles Bibliográficos
Autores principales:	Roshan, Mascarenhas, Vijaya, Pai H., Lavanya, G. Rao, Shama, Prasada K., Santhiya, S.T., Graw, Jochen, Gopinath, P.M., Satyamoorthy, K.
Formato:	Texto
Lenguaje:	English
Publicado:	Molecular Vision 2010
Materias:	Research Article
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2875257/ https://www.ncbi.nlm.nih.gov/pubmed/20508808

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