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Journal Abstract Search

409 related items for PubMed ID: 23571586

  • 21. A hERG mutation E1039X produced a synergistic lesion on IKs together with KCNQ1-R174C mutation in a LQTS family with three compound mutations.
    Wu J, Mizusawa Y, Ohno S, Ding WG, Higaki T, Wang Q, Kohjitani H, Makiyama T, Itoh H, Toyoda F, James AF, Hancox JC, Matsuura H, Horie M.
    Sci Rep; 2018 Feb 15; 8(1):3129. PubMed ID: 29449639
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  • 22. Overlapping LQT1 and LQT2 phenotype in a patient with long QT syndrome associated with loss-of-function variations in KCNQ1 and KCNH2.
    Cordeiro JM, Perez GJ, Schmitt N, Pfeiffer R, Nesterenko VV, Burashnikov E, Veltmann C, Borggrefe M, Wolpert C, Schimpf R, Antzelevitch C.
    Can J Physiol Pharmacol; 2010 Dec 15; 88(12):1181-90. PubMed ID: 21164565
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  • 25. Genetics of long QT syndrome.
    Tester DJ, Ackerman MJ.
    Methodist Debakey Cardiovasc J; 2014 Dec 15; 10(1):29-33. PubMed ID: 24932360
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  • 29. N- and C-terminal KCNE1 mutations cause distinct phenotypes of long QT syndrome.
    Ohno S, Zankov DP, Yoshida H, Tsuji K, Makiyama T, Itoh H, Akao M, Hancox JC, Kita T, Horie M.
    Heart Rhythm; 2007 Mar 15; 4(3):332-40. PubMed ID: 17341399
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  • 33. Postmortem long QT syndrome genetic testing for sudden unexplained death in the young.
    Tester DJ, Ackerman MJ.
    J Am Coll Cardiol; 2007 Jan 16; 49(2):240-6. PubMed ID: 17222736
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  • 37. Genetic variations of KCNQ1, KCNH2, SCN5A, KCNE1, and KCNE2 in drug-induced long QT syndrome patients.
    Paulussen AD, Gilissen RA, Armstrong M, Doevendans PA, Verhasselt P, Smeets HJ, Schulze-Bahr E, Haverkamp W, Breithardt G, Cohen N, Aerssens J.
    J Mol Med (Berl); 2004 Mar 16; 82(3):182-8. PubMed ID: 14760488
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  • 40. Mutation analysis in congenital Long QT Syndrome--a case with missense mutations in KCNQ1 and SCN5A.
    Paulussen A, Matthijs G, Gewillig M, Verhasselt P, Cohen N, Aerssens J.
    Genet Test; 2003 Mar 16; 7(1):57-61. PubMed ID: 12820704
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