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Bestrophinopathy: An RPE-Photoreceptor Interface Disease
Bestrophinopathies, one of the most common forms of inherited macular degenerations, are caused by mutations in the BEST1 gene expressed in the retinal pigment epithelium (RPE). Both human and canine BEST1-linked maculopathies are characterized by abnormal accumulation of autofluorescent material wi...
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| Veröffentlicht in: | Prog Retin Eye Res |
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| Hauptverfasser: | , , , , , , , , , , |
| Format: | Artigo |
| Sprache: | Inglês |
| Veröffentlicht: |
2017
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| Schlagworte: | |
| Online Zugang: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5441932/ https://ncbi.nlm.nih.gov/pubmed/28111324 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.preteyeres.2017.01.005 |
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