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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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| Udgivet i: | Prog Retin Eye Res |
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| Main Authors: | , , , , , , |
| Format: | Artigo |
| Sprog: | Inglês |
| Udgivet: |
2017
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| 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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