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A novel MIP gene mutation associated with autosomal dominant congenital cataracts in a Chinese family
BACKGROUND: The major intrinsic protein gene (MIP), also known as MIP26 or AQP0, is a member of the water-transporting aquaporin family, which plays a critical role in the maintenance of lifelong lens transparency. To date, several mutations in MIP (OMIM 154050) have been linked to hereditary catara...
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| Main Authors: | , , , , , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
BioMed Central
2014
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3890554/ https://ncbi.nlm.nih.gov/pubmed/24405844 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/1471-2350-15-6 |
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