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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Detalles Bibliográficos
Autores principales: Milenkovic, Vladimir M, Langmann, Thomas, Schreiber, Rainer, Kunzelmann, Karl, Weber, Bernhard HF
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2008
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2292144/
https://www.ncbi.nlm.nih.gov/pubmed/18307799
http://dx.doi.org/10.1186/1471-2148-8-72

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2292144/
https://www.ncbi.nlm.nih.gov/pubmed/18307799
http://dx.doi.org/10.1186/1471-2148-8-72

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