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Journal Abstract Search

150 related items for PubMed ID: 10634626

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  • 2. Analysis of the Stargardt disease gene (ABCR) in age-related macular degeneration.
    De La Paz MA, Guy VK, Abou-Donia S, Heinis R, Bracken B, Vance JM, Gilbert JR, Gass JD, Haines JL, Pericak-Vance MA.
    Ophthalmology; 1999 Aug; 106(8):1531-6. PubMed ID: 10442900
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  • 3. New ABCR mutations and clinical phenotype in Italian patients with Stargardt disease.
    Simonelli F, Testa F, de Crecchio G, Rinaldi E, Hutchinson A, Atkinson A, Dean M, D'Urso M, Allikmets R.
    Invest Ophthalmol Vis Sci; 2000 Mar; 41(3):892-7. PubMed ID: 10711710
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  • 4. Age-related macular degeneration in grandparents of patients with Stargardt disease: genetic study.
    Souied EH, Ducroq D, Gerber S, Ghazi I, Rozet JM, Perrault I, Munnich A, Dufier JL, Coscas G, Soubrane G, Kaplan J.
    Am J Ophthalmol; 1999 Aug; 128(2):173-8. PubMed ID: 10458172
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  • 5. A novel ABCR nonsense mutation responsible for late-onset fundus flavimaculatus.
    Souied EH, Ducroq D, Rozet JM, Gerber S, Perrault I, Sterkers M, Benhamou N, Munnich A, Coscas G, Soubrane G, Kaplan J.
    Invest Ophthalmol Vis Sci; 1999 Oct; 40(11):2740-4. PubMed ID: 10509673
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  • 12. ATP binding cassette transporter retina genotypes and age related macular degeneration: an analysis on exudative non-familial Japanese patients.
    Kuroiwa S, Kojima H, Kikuchi T, Yoshimura N.
    Br J Ophthalmol; 1999 May; 83(5):613-5. PubMed ID: 10216065
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  • 13. The rod photoreceptor ATP-binding cassette transporter gene, ABCR, and retinal disease: from monogenic to multifactorial.
    Shroyer NF, Lewis RA, Allikmets R, Singh N, Dean M, Leppert M, Lupski JR.
    Vision Res; 1999 Jul; 39(15):2537-44. PubMed ID: 10396622
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  • 15. Autosomal recessive retinitis pigmentosa and cone-rod dystrophy caused by splice site mutations in the Stargardt's disease gene ABCR.
    Cremers FP, van de Pol DJ, van Driel M, den Hollander AI, van Haren FJ, Knoers NV, Tijmes N, Bergen AA, Rohrschneider K, Blankenagel A, Pinckers AJ, Deutman AF, Hoyng CB.
    Hum Mol Genet; 1998 Mar; 7(3):355-62. PubMed ID: 9466990
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  • 17. Cosegregation and functional analysis of mutant ABCR (ABCA4) alleles in families that manifest both Stargardt disease and age-related macular degeneration.
    Shroyer NF, Lewis RA, Yatsenko AN, Wensel TG, Lupski JR.
    Hum Mol Genet; 2001 Nov 01; 10(23):2671-8. PubMed ID: 11726554
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  • 19. The ABCR gene in recessive and dominant Stargardt diseases: a genetic pathway in macular degeneration.
    Zhang K, Kniazeva M, Hutchinson A, Han M, Dean M, Allikmets R.
    Genomics; 1999 Sep 01; 60(2):234-7. PubMed ID: 10486215
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