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Journal Abstract Search

190 related items for PubMed ID: 15031171

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  • 2. Mutational analysis of RPGR and RP2 genes in Japanese patients with retinitis pigmentosa: identification of four mutations.
    Jin ZB, Liu XQ, Hayakawa M, Murakami A, Nao-i N.
    Mol Vis; 2006 Oct 06; 12():1167-74. PubMed ID: 17093403
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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 06; 41(9):2712-21. PubMed ID: 10937588
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  • 4. RP2 phenotype and pathogenetic correlations in X-linked retinitis pigmentosa.
    Jayasundera T, Branham KE, Othman M, Rhoades WR, Karoukis AJ, Khanna H, Swaroop A, Heckenlively JR.
    Arch Ophthalmol; 2010 Jul 06; 128(7):915-23. PubMed ID: 20625056
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  • 8. Screening for mutations in RPGR and RP2 genes in Jordanian families with X-linked retinitis pigmentosa.
    Haddad MF, Khabour OF, Abuzaideh KA, Shihadeh W.
    Genet Mol Res; 2016 Jun 03; 15(2):. PubMed ID: 27323122
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  • 13. A new 2-base pair deletion in the RPGR gene in a black family with X-linked retinitis pigmentosa.
    Fishman GA, Grover S, Buraczynska M, Wu W, Swaroop A.
    Arch Ophthalmol; 1998 Feb 03; 116(2):213-8. PubMed ID: 9488274
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  • 14. Novel mutation in RP2 gene in two brothers with X-linked retinitis pigmentosa and mtDNA mutation of leber hereditary optic neuropathy who showed marked differences in clinical severity.
    Mashima Y, Saga M, Hiida Y, Imamura Y, Kudoh J, Shimizu N.
    Am J Ophthalmol; 2000 Sep 03; 130(3):357-9. PubMed ID: 11020419
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