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Journal Abstract Search

312 related items for PubMed ID: 9354802

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  • 2. Properties of KvLQT1 K+ channel mutations in Romano-Ward and Jervell and Lange-Nielsen inherited cardiac arrhythmias.
    Chouabe C, Neyroud N, Guicheney P, Lazdunski M, Romey G, Barhanin J.
    EMBO J; 1997 Sep 01; 16(17):5472-9. PubMed ID: 9312006
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  • 3. Dysfunction of delayed rectifier potassium channels in an inherited cardiac arrhythmia.
    Sanguinetti MC.
    Ann N Y Acad Sci; 1999 Apr 30; 868():406-13. PubMed ID: 10414310
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  • 6. A novel long-QT 5 gene mutation in the C-terminus (V109I) is associated with a mild phenotype.
    Schulze-Bahr E, Schwarz M, Hauenschild S, Wedekind H, Funke H, Haverkamp W, Breithardt G, Pongs O, Isbrandt D.
    J Mol Med (Berl); 2001 Sep 30; 79(9):504-9. PubMed ID: 11692163
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  • 7. Compound heterozygous mutations in KvLQT1 cause Jervell and Lange-Nielsen syndrome.
    Wang Z, Li H, Moss AJ, Robinson J, Zareba W, Knilans T, Bowles NE, Towbin JA.
    Mol Genet Metab; 2002 Apr 30; 75(4):308-16. PubMed ID: 12051962
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  • 9. Clinical and electrophysiological characterization of a novel mutation (F193L) in the KCNQ1 gene associated with long QT syndrome.
    Yamaguchi M, Shimizu M, Ino H, Terai H, Hayashi K, Mabuchi H, Hoshi N, Higashida H.
    Clin Sci (Lond); 2003 Apr 30; 104(4):377-82. PubMed ID: 12653681
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  • 12. Biophysical characteristics of a new mutation on the KCNQ1 potassium channel (L251P) causing long QT syndrome.
    Deschênes D, Acharfi S, Pouliot V, Hegele R, Krahn A, Daleau P, Chahine M.
    Can J Physiol Pharmacol; 2003 Feb 30; 81(2):129-34. PubMed ID: 12710526
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  • 15. The G314S KCNQ1 mutation exerts a dominant-negative effect on expression of KCNQ1 channels in oocytes.
    Li W, Du R, Wang QF, Tian L, Yang JG, Song ZF.
    Biochem Biophys Res Commun; 2009 May 29; 383(2):206-9. PubMed ID: 19348785
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  • 17. Heterozygous mutation in the pore of potassium channel gene KvLQT1 causes an apparently normal phenotype in long QT syndrome.
    Neyroud N, Denjoy I, Donger C, Gary F, Villain E, Leenhardt A, Benali K, Schwartz K, Coumel P, Guicheney P.
    Eur J Hum Genet; 1998 May 29; 6(2):129-33. PubMed ID: 9781056
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  • 20. Genomic structure of three long QT syndrome genes: KVLQT1, HERG, and KCNE1.
    Splawski I, Shen J, Timothy KW, Vincent GM, Lehmann MH, Keating MT.
    Genomics; 1998 Jul 01; 51(1):86-97. PubMed ID: 9693036
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