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Journal Abstract Search

266 related items for PubMed ID: 11726554

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  • 4. Biochemical defects in ABCR protein variants associated with human retinopathies.
    Sun H, Smallwood PM, Nathans J.
    Nat Genet; 2000 Oct; 26(2):242-6. PubMed ID: 11017087
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  • 5. Three families displaying the combination of Stargardt's disease with cone-rod dystrophy or retinitis pigmentosa.
    Klevering BJ, Maugeri A, Wagner A, Go SL, Vink C, Cremers FP, Hoyng CB.
    Ophthalmology; 2004 Mar; 111(3):546-53. PubMed ID: 15019334
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  • 10. Analysis of ABCA4 in mixed Spanish families segregating different retinal dystrophies.
    Paloma E, Coco R, Martínez-Mir A, Vilageliu L, Balcells S, Gonzàlez-Duarte R.
    Hum Mutat; 2002 Dec; 20(6):476. PubMed ID: 12442277
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  • 11. ABCA4 gene mutations in Japanese patients with Stargardt disease and retinitis pigmentosa.
    Fukui T, Yamamoto S, Nakano K, Tsujikawa M, Morimura H, Nishida K, Ohguro N, Fujikado T, Irifune M, Kuniyoshi K, Okada AA, Hirakata A, Miyake Y, Tano Y.
    Invest Ophthalmol Vis Sci; 2002 Sep; 43(9):2819-24. PubMed ID: 12202497
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  • 15. Mutations of the retinal specific ATP binding transporter gene (ABCR) in a single family segregating both autosomal recessive retinitis pigmentosa RP19 and Stargardt disease: evidence of clinical heterogeneity at this locus.
    Rozet JM, Gerber S, Ghazi I, Perrault I, Ducroq D, Souied E, Cabot A, Dufier JL, Munnich A, Kaplan J.
    J Med Genet; 1999 Jun; 36(6):447-51. PubMed ID: 10874631
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  • 16. ABCR unites what ophthalmologists divide(s).
    van Driel MA, Maugeri A, Klevering BJ, Hoyng CB, Cremers FP.
    Ophthalmic Genet; 1998 Sep; 19(3):117-22. PubMed ID: 9810566
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  • 19. An ABCA4 genomic deletion in patients with Stargardt disease.
    Yatsenko AN, Shroyer NF, Lewis RA, Lupski JR.
    Hum Mutat; 2003 Jun; 21(6):636-44. PubMed ID: 12754711
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