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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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| Main Authors: | , , , , , , , , , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado: |
BMJ Group
2005
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| Assuntos: | |
| Acceso en liña: | 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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