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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Main Authors: Aleman, Tomas S., Cideciyan, Artur V., Sumaroka, Alexander, Schwartz, Sharon B., Roman, Alejandro J., Windsor, Elizabeth A. M., Steinberg, Janet D., Branham, Kari, Othman, Mohammad, Swaroop, Anand, Jacobson, Samuel G.
Format: Artigo
Language:Inglês
Published: Association for Research in Vision and Ophthalmology 2007
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Online Access: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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