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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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| Publicado en: | Prog Retin Eye Res |
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| Main Authors: | , , , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado: |
2017
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| Assuntos: | |
| Acceso en liña: | 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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