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Inner Retinal Abnormalities in X-linked Retinitis Pigmentosa with RPGR Mutations
Purpose. To investigate in vivo the retinal microstructure in X-linked retinitis pigmentosa (XLRP) caused by RPGR mutations as a prelude to treatment initiatives for this common form of RP. Methods. Patients with RPGR-XLRP (n = 12; age range, 10–56 years) were studied by optical coherence tomography...
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| Hauptverfasser: | , , , , , , , , , , |
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| Format: | Artigo |
| Sprache: | Inglês |
| Veröffentlicht: |
Association for Research in Vision and Ophthalmology
2007
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| Schlagworte: | |
| Online Zugang: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3178894/ https://ncbi.nlm.nih.gov/pubmed/17898302 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1167/iovs.07-0453 |
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