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Journal Abstract Search

146 related items for PubMed ID: 15627199

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  • 2. [Function of bestrophin].
    Strauss O, Rosenthal R.
    Ophthalmologe; 2005 Feb; 102(2):122-6. PubMed ID: 15627200
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  • 5. Mutations in a novel gene, VMD2, encoding a protein of unknown properties cause juvenile-onset vitelliform macular dystrophy (Best's disease).
    Marquardt A, Stöhr H, Passmore LA, Krämer F, Rivera A, Weber BH.
    Hum Mol Genet; 1998 Sep; 7(9):1517-25. PubMed ID: 9700209
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  • 6. The mutation spectrum of the bestrophin protein--functional implications.
    Bakall B, Marknell T, Ingvast S, Koisti MJ, Sandgren O, Li W, Bergen AA, Andreasson S, Rosenberg T, Petrukhin K, Wadelius C.
    Hum Genet; 1999 May; 104(5):383-9. PubMed ID: 10394929
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  • 8. Mutations of VMD2 splicing regulators cause nanophthalmos and autosomal dominant vitreoretinochoroidopathy (ADVIRC).
    Yardley J, Leroy BP, Hart-Holden N, Lafaut BA, Loeys B, Messiaen LM, Perveen R, Reddy MA, Bhattacharya SS, Traboulsi E, Baralle D, De Laey JJ, Puech B, Kestelyn P, Moore AT, Manson FD, Black GC.
    Invest Ophthalmol Vis Sci; 2004 Oct; 45(10):3683-9. PubMed ID: 15452077
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  • 9. VMD2 mutations in vitelliform macular dystrophy (Best disease) and other maculopathies.
    White K, Marquardt A, Weber BH.
    Hum Mutat; 2000 Oct; 15(4):301-8. PubMed ID: 10737974
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  • 12. The gene causing the Best's macular dystrophy (BMD) encodes a putative ion exchanger.
    Gómez A, Cedano J, Oliva B, Piñol J, Querol E.
    DNA Seq; 2001 Dec; 12(5-6):431-5. PubMed ID: 11913792
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  • 18. Identification of novel VMD2 gene mutations in patients with best vitelliform macular dystrophy.
    Marchant D, Gogat K, Boutboul S, Péquignot M, Sternberg C, Dureau P, Roche O, Uteza Y, Hache JC, Puech B, Puech V, Dumur V, Mouillon M, Munier FL, Schorderet DF, Marsac C, Dufier JL, Abitbol M.
    Hum Mutat; 2001 Mar; 17(3):235. PubMed ID: 11241846
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  • 20. Best's vitelliform macular dystrophy caused by a new mutation (Val89Ala) in the VMD2 gene.
    Eksandh L, Bakall B, Bauer B, Wadelius C, Andréasson S.
    Ophthalmic Genet; 2001 Jun; 22(2):107-15. PubMed ID: 11449320
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