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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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| Main Authors: | , , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Nature Publishing Group
2011
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| Assuntos: | |
| Acesso em linha: | 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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