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Congenital progressive polymorphic cataract caused by a mutation in the major intrinsic protein of the lens, MIP (AQP0)
BACKGROUND—Congenital cataract, when inherited as an isolated abnormality, is phenotypically and genetically heterogeneous. Although there is no agreed nomenclature for the patterns of cataract observed, a recent study identified eight readily identifiable phenotypes. METHODS—The Moorfields Eye Hosp...
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| Main Authors: | , , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
2000
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC1723363/ https://ncbi.nlm.nih.gov/pubmed/11090476 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1136/bjo.84.12.1376 |
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