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2. Novel mutations of RPGR in Chinese families with X-linked retinitis pigmentosa. Zhang Z, Dai H, Wang L, Tao T, Xu J, Sun X, Yang L, Li G. BMC Ophthalmol; 2019 Nov 27; 19(1):240. PubMed ID: 31775781 [Abstract] [Full Text] [Related]
3. Novel RPGR-ORF15 mutations in X-linked retinitis pigmentosa patients. Gan DK, He CL, Shu HR, Hoffman MR, Jin ZB. Neurosci Lett; 2011 Aug 01; 500(1):16-9. PubMed ID: 21683121 [Abstract] [Full Text] [Related]
14. X-linked retinitis pigmentosa: RPGR mutations in most families with definite X linkage and clustering of mutations in a short sequence stretch of exon ORF15. Bader I, Brandau O, Achatz H, Apfelstedt-Sylla E, Hergersberg M, Lorenz B, Wissinger B, Wittwer B, Rudolph G, Meindl A, Meitinger T. Invest Ophthalmol Vis Sci; 2003 Apr 01; 44(4):1458-63. PubMed ID: 12657579 [Abstract] [Full Text] [Related]
16. X-linked retinitis pigmentosa in two families with a missense mutation in the RPGR gene and putative change of glycine to valine at codon 60. Fishman GA, Grover S, Jacobson SG, Alexander KR, Derlacki DJ, Wu W, Buraczynska M, Swaroop A. Ophthalmology; 1998 Dec 01; 105(12):2286-96. PubMed ID: 9855162 [Abstract] [Full Text] [Related]
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