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A novel mutation in CRYAB associated with autosomal dominant congenital nuclear cataract in a Chinese family

PURPOSE: To identify the genetic defects associated with autosomal dominant congenital nuclear cataract in a Chinese family. METHODS: Clinical data were collected, and the phenotypes of the affected members in this family were recorded by slit-lamp photography. Genomic DNA was isolated from peripher...

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Bibliografiske detaljer
Main Authors: Chen, Qiang, Ma, Junjie, Yan, Ming, Mothobi, Maneo Emily, Liu, Yuanyuan, Zheng, Fang
Format: Artigo
Sprog:Inglês
Udgivet: Molecular Vision 2009
Fag:
Online adgang:https://ncbi.nlm.nih.gov/pmc/articles/PMC2709425/
https://ncbi.nlm.nih.gov/pubmed/19597569
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