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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Autors principals: Milenkovic, Vladimir M, Langmann, Thomas, Schreiber, Rainer, Kunzelmann, Karl, Weber, Bernhard HF
Format: Artigo
Idioma:Inglês
Publicat: BioMed Central 2008
Matèries:
Research Article
Accés en línia: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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