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Journal Abstract Search

380 related items for PubMed ID: 11968081

  • 21.
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  • 22. A population-based epidemiological and genetic study of X-linked retinitis pigmentosa.
    Prokisch H, Hartig M, Hellinger R, Meitinger T, Rosenberg T.
    Invest Ophthalmol Vis Sci; 2007 Sep; 48(9):4012-8. PubMed ID: 17724181
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  • 23.
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  • 24. The retinitis pigmentosa GTPase regulator (RPGR) interacts with novel transport-like proteins in the outer segments of rod photoreceptors.
    Roepman R, Bernoud-Hubac N, Schick DE, Maugeri A, Berger W, Ropers HH, Cremers FP, Ferreira PA.
    Hum Mol Genet; 2000 Sep 01; 9(14):2095-105. PubMed ID: 10958648
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  • 25. Evaluation of RP2 and RP3 genes in an X-linked RP family manifesting loss of central vision and preserved peripheral function.
    Hiraoka M, Trese MT, Shastry BS.
    J Hum Genet; 2001 Sep 01; 46(4):241-3. PubMed ID: 11322665
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  • 27. 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
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  • 28. Histopathologic study of X-linked cone-rod dystrophy (CORDX1) caused by a mutation in the RPGR exon ORF15.
    Demirci FY, Gupta N, Radak AL, Rigatti BW, Mah TS, Milam AH, Gorin MB.
    Am J Ophthalmol; 2005 Feb 01; 139(2):386-8. PubMed ID: 15734019
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  • 29. X-linked cone-rod dystrophy (locus COD1): identification of mutations in RPGR exon ORF15.
    Demirci FY, Rigatti BW, Wen G, Radak AL, Mah TS, Baic CL, Traboulsi EI, Alitalo T, Ramser J, Gorin MB.
    Am J Hum Genet; 2002 Apr 01; 70(4):1049-53. PubMed ID: 11857109
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  • 32. X-linked retinitis pigmentosa associated with a 2-base pair insertion in codon 99 of the RP3 gene RPGR.
    Weleber RG, Butler NS, Murphey WH, Sheffield VC, Stone EM.
    Arch Ophthalmol; 1997 Nov 01; 115(11):1429-35. PubMed ID: 9366675
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  • 33.
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  • 35. Disease course of patients with X-linked retinitis pigmentosa due to RPGR gene mutations.
    Sandberg MA, Rosner B, Weigel-DiFranco C, Dryja TP, Berson EL.
    Invest Ophthalmol Vis Sci; 2007 Mar 01; 48(3):1298-304. PubMed ID: 17325176
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  • 37. Novel mutations of the RPGR gene in RP3 families.
    Zito I, Gorin MB, Plant C, Bird AC, Bhattacharya SS, Hardcastle AJ.
    Hum Mutat; 2000 Apr 01; 15(4):386. PubMed ID: 10737996
    [Abstract] [Full Text] [Related]

  • 38. Discordant phenotypes in fraternal twins having an identical mutation in exon ORF15 of the RPGR gene.
    Walia S, Fishman GA, Swaroop A, Branham KE, Lindeman M, Othman M, Weleber RG.
    Arch Ophthalmol; 2008 Mar 01; 126(3):379-84. PubMed ID: 18332319
    [Abstract] [Full Text] [Related]

  • 39. Spectrum of mutations in the RPGR gene that are identified in 20% of families with X-linked retinitis pigmentosa.
    Buraczynska M, Wu W, Fujita R, Buraczynska K, Phelps E, Andréasson S, Bennett J, Birch DG, Fishman GA, Hoffman DR, Inana G, Jacobson SG, Musarella MA, Sieving PA, Swaroop A.
    Am J Hum Genet; 1997 Dec 01; 61(6):1287-92. PubMed ID: 9399904
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  • 40.
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