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Molecular evolution and functional divergence of the bestrophin protein family
BACKGROUND: Mutations in human bestrophin 1 are associated with at least three autosomal-dominant macular dystrophies including Best disease, adult onset vitelliform macular dystrophy and autosomal dominant vitreo-retinochoroidopathy. The protein is integral to the membrane and is likely involved in...
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| Main Authors: | , , , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
BioMed Central
2008
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC2292144/ https://ncbi.nlm.nih.gov/pubmed/18307799 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/1471-2148-8-72 |
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