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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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Bibliografiske detaljer
Udgivet i: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.
Format: Artigo
Sprog:Inglês
Udgivet: 2017
Fag:
Online adgang: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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