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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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Bibliografske podrobnosti
izdano v: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
Jezik:Inglês
Izdano: 2017
Teme:
Online dostop: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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