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Bestrophin 1 and Retinal Disease

Mutations in the gene BEST1 are causally associated with as many as five clinically distinct retinal degenerative diseases, which are collectively referred to as the “bestrophinopathies”. These five associated diseases are: Best vitelliform macular dystrophy, autosomal recessive bestrophinopathy, ad...

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Detalhes bibliográficos
Publicado no:Prog Retin Eye Res
Main Authors: Johnson, Adiv A., Guziewicz, Karina E., Lee, C. Justin, Kalathar, Ravi C., Pulido, Jose S., Marmorstein, Lihua Y., Marmorstein, Alan D.
Formato: Artigo
Idioma:Inglês
Publicado em: 2017
Assuntos:
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC5600499/
https://ncbi.nlm.nih.gov/pubmed/28153808
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.preteyeres.2017.01.006
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