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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Main Authors: Roshan, Mascarenhas, Vijaya, Pai H., Lavanya, G. Rao, Shama, Prasada K., Santhiya, S.T., Graw, Jochen, Gopinath, P.M., Satyamoorthy, K.
Format: Artigo
Jezik:Inglês
Izdano: Molecular Vision 2010
Teme:
Research Article
Online dostop:https://ncbi.nlm.nih.gov/pmc/articles/PMC2875257/
https://ncbi.nlm.nih.gov/pubmed/20508808
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