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...

Descripción completa

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

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2875257/
https://www.ncbi.nlm.nih.gov/pubmed/20508808

Ejemplares similares