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Spectrum of rhodopsin mutations in French autosomal dominant rod-cone dystrophy patients
PURPOSE: To identify the prevalence of rhodopsin (RHO) mutations in French patients with autosomal dominant rod-cone dystrophies (adRP). METHODS: Detailed phenotypic characterization was performed including precise family history, best corrected visual acuity using the ETDRS chart, slit lamp examina...
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| Glavni autori: | , , , , , , , , , , , , |
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| Format: | Artigo |
| Jezik: | Inglês |
| Izdano: |
Association for Research in Vision and Ophthalmology
2010
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| Teme: | |
| Online pristup: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3102265/ https://ncbi.nlm.nih.gov/pubmed/20164459 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1167/iovs.09-4766 |
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