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PUBMED FOR HANDHELDS

Journal Abstract Search


136 related items for PubMed ID: 11798852

  • 1. [Identification of a nonsense mutation causing X-linked RP2 in two Chinese families].
    Liu L, Wei Y, Chen H.
    Zhonghua Yi Xue Za Zhi; 2001 Jan 25; 81(2):71-2. PubMed ID: 11798852
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  • 2. Identification of novel RP2 mutations in a subset of X-linked retinitis pigmentosa families and prediction of new domains.
    Miano MG, Testa F, Filippini F, Trujillo M, Conte I, Lanzara C, Millán JM, De Bernardo C, Grammatico B, Mangino M, Torrente I, Carrozzo R, Simonelli F, Rinaldi E, Ventruto V, D'Urso M, Ayuso C, Ciccodicola A.
    Hum Mutat; 2001 Aug 25; 18(2):109-19. PubMed ID: 11462235
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  • 3. X-linked retinitis pigmentosa: mutation spectrum of the RPGR and RP2 genes and correlation with visual function.
    Sharon D, Bruns GA, McGee TL, Sandberg MA, Berson EL, Dryja TP.
    Invest Ophthalmol Vis Sci; 2000 Aug 25; 41(9):2712-21. PubMed ID: 10937588
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  • 5. Mutational screening of the RP2 and RPGR genes in Spanish families with X-linked retinitis pigmentosa.
    García-Hoyos M, Garcia-Sandoval B, Cantalapiedra D, Riveiro R, Lorda-Sánchez I, Trujillo-Tiebas MJ, Rodriguez de Alba M, Millan JM, Baiget M, Ramos C, Ayuso C.
    Invest Ophthalmol Vis Sci; 2006 Sep 25; 47(9):3777-82. PubMed ID: 16936086
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  • 6. Three novel mutations of the RPGR gene exon ORF15 in three Japanese families with X-linked retinitis pigmentosa.
    Yokoyama A, Maruiwa F, Hayakawa M, Kanai A, Vervoort R, Wright AF, Yamada K, Niikawa N, Naōi N.
    Am J Med Genet; 2001 Dec 01; 104(3):232-8. PubMed ID: 11754050
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  • 7. Identification of an intronic single-point mutation in RP2 as the cause of semidominant X-linked retinitis pigmentosa.
    Pomares E, Riera M, Castro-Navarro J, Andrés-Gutiérrez A, Gonzàlez-Duarte R, Marfany G.
    Invest Ophthalmol Vis Sci; 2009 Nov 01; 50(11):5107-14. PubMed ID: 19516003
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  • 11. [Gene diagnosis of X linked retinitis pigmentosa by linkage analysis].
    Liu M, Wei Y, Liu L.
    Zhonghua Yi Xue Za Zhi; 1999 Jan 01; 79(1):54-6. PubMed ID: 11601008
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  • 13. 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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  • 14. A novel RPGR gene mutation in a Chinese family with X-linked dominant retinitis pigmentosa.
    Li Y, Dong B, Hu AL, Cui TT, Zheng YY.
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2005 Aug 01; 22(4):396-8. PubMed ID: 16086276
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  • 16. Delineation of the plasma membrane targeting domain of the X-linked retinitis pigmentosa protein RP2.
    Chapple JP, Hardcastle AJ, Grayson C, Willison KR, Cheetham ME.
    Invest Ophthalmol Vis Sci; 2002 Jun 01; 43(6):2015-20. PubMed ID: 12037013
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  • 17. Three novel mutations causing a truncated protein within the RP2 gene in Italian families with X-linked retinitis pigmentosa.
    De Luca A, Torrente I, Mangino M, Danesi R, Dallapiccola B, Novelli G.
    Mutat Res; 2001 Jan 01; 432(3-4):79-82. PubMed ID: 11465545
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  • 18. 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 01; 48(9):4012-8. PubMed ID: 17724181
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  • 19. Positional cloning of the gene for X-linked retinitis pigmentosa 2.
    Schwahn U, Lenzner S, Dong J, Feil S, Hinzmann B, van Duijnhoven G, Kirschner R, Hemberger M, Bergen AA, Rosenberg T, Pinckers AJ, Fundele R, Rosenthal A, Cremers FP, Ropers HH, Berger W.
    Nat Genet; 1998 Aug 01; 19(4):327-32. PubMed ID: 9697692
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