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Two-year progression analysis of RPE65 autosomal dominant retinitis pigmentosa
BACKGROUND: The RPE65 gene was recently described to cause autosomal dominant retinitis pigmentosa (adRP), presenting with a phenotype resembling choroideremia. This study presents the 2-year progression of RPE65 adRP in a patient. METHODS: This is an observational case report of one patient. The pa...
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| Gepubliceerd in: | Ophthalmic Genet |
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| Hoofdauteurs: | , , |
| Formaat: | Artigo |
| Taal: | Inglês |
| Gepubliceerd in: |
2018
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| Onderwerpen: | |
| Online toegang: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6314189/ https://ncbi.nlm.nih.gov/pubmed/29947567 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1080/13816810.2018.1484929 |
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