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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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| 主要な著者: | , , , , |
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| フォーマット: | Artigo |
| 言語: | Inglês |
| 出版事項: |
BioMed Central
2008
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| 主題: | |
| オンライン･アクセス: | 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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