A novel locus for autosomal dominant congenital cerulean cataract maps to chromosome 12q

Cataracts are the commonest cause of blindness worldwide. Inherited cataract is a clinically and genetically heterogeneous disease that most often shows autosomal dominant inheritance. In this study, we report the identification of a novel locus for cerulean cataract type 5 (CCA5), also known as blu...

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Bibliographic Details
Main Authors: Berry, Vanita, Ionides, Alexander C W, Moore, Anthony T, Bhattacharya, Shomi S
Format: Artigo
Language:Inglês
Published: Nature Publishing Group 2011
Subjects:
Short Report
Online Access:https://ncbi.nlm.nih.gov/pmc/articles/PMC3230366/
https://ncbi.nlm.nih.gov/pubmed/21731060
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1038/ejhg.2011.130
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