Gamma-S crystallin gene (CRYGS) mutation causes dominant progressive cortical cataract in humans

Background: Congenital or childhood cataract is clinically and genetically a highly heterogeneous lens disorder in children. Autosomal dominant inheritance is most common. Objective: To report the identification of a mutation in the human CRYGS gene. Subjects and methods: A large six generation fami...

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Detalhes bibliográficos
Main Authors: Sun, H, Ma, Z, Li, Y, Liu, B, Li, Z, Ding, X, Gao, Y, Ma, W, Tang, X, Li, X, Shen, Y
Formato: Artigo
Idioma:Inglês
Publicado em: BMJ Group 2005
Assuntos:
Short Report
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC1736139/
https://ncbi.nlm.nih.gov/pubmed/16141006
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1136/jmg.2004.028274
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