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Journal Abstract Search

703 related items for PubMed ID: 22882672

  • 1. The prevalence of mutations in KCNQ1, KCNH2, and SCN5A in an unselected national cohort of young sudden unexplained death cases.
    Winkel BG, Larsen MK, Berge KE, Leren TP, Nissen PH, Olesen MS, Hollegaard MV, Jespersen T, Yuan L, Nielsen N, Haunsø S, Svendsen JH, Wang Y, Kristensen IB, Jensen HK, Tfelt-Hansen J, Banner J.
    J Cardiovasc Electrophysiol; 2012 Oct; 23(10):1092-8. PubMed ID: 22882672
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  • 2. Mutation Analysis of KCNQ1, KCNH2 and SCN5A Genes in Taiwanese Long QT Syndrome Patients.
    Chang YS, Yang YW, Lin YN, Lin KH, Chang KC, Chang JG.
    Int Heart J; 2015 Oct; 56(4):450-3. PubMed ID: 26118593
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  • 3. Long QT syndrome-associated mutations in intrauterine fetal death.
    Crotti L, Tester DJ, White WM, Bartos DC, Insolia R, Besana A, Kunic JD, Will ML, Velasco EJ, Bair JJ, Ghidoni A, Cetin I, Van Dyke DL, Wick MJ, Brost B, Delisle BP, Facchinetti F, George AL, Schwartz PJ, Ackerman MJ.
    JAMA; 2013 Apr 10; 309(14):1473-82. PubMed ID: 23571586
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  • 4. Long QT and Brugada syndrome gene mutations in New Zealand.
    Chung SK, MacCormick JM, McCulley CH, Crawford J, Eddy CA, Mitchell EA, Shelling AN, French JK, Skinner JR, Rees MI.
    Heart Rhythm; 2007 Oct 10; 4(10):1306-14. PubMed ID: 17905336
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  • 5. Investigation of ion channel gene variants in patients with long QT syndrome.
    Ernesto C, Cruz FE, Lima FS, Coutinho JL, Silva R, Urményi TP, Carvalho AC, Rondinelli E.
    Arq Bras Cardiol; 2011 Mar 10; 96(3):172-8. PubMed ID: 21308345
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  • 6. Whole-Exome Molecular Autopsy After Exertion-Related Sudden Unexplained Death in the Young.
    Anderson JH, Tester DJ, Will ML, Ackerman MJ.
    Circ Cardiovasc Genet; 2016 Jun 10; 9(3):259-65. PubMed ID: 27114410
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  • 11. Screening for copy number variation in genes associated with the long QT syndrome: clinical relevance.
    Barc J, Briec F, Schmitt S, Kyndt F, Le Cunff M, Baron E, Vieyres C, Sacher F, Redon R, Le Caignec C, Le Marec H, Probst V, Schott JJ.
    J Am Coll Cardiol; 2011 Jan 04; 57(1):40-7. PubMed ID: 21185499
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  • 12. Allelic dropout in long QT syndrome genetic testing: a possible mechanism underlying false-negative results.
    Tester DJ, Cronk LB, Carr JL, Schulz V, Salisbury BA, Judson RS, Ackerman MJ.
    Heart Rhythm; 2006 Jul 04; 3(7):815-21. PubMed ID: 16818214
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  • 13. 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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  • 14. Protective effect of KCNH2 single nucleotide polymorphism K897T in LQTS families and identification of novel KCNQ1 and KCNH2 mutations.
    Zhang X, Chen S, Zhang L, Liu M, Redfearn S, Bryant RM, Oberti C, Vincent GM, Wang QK.
    BMC Med Genet; 2008 Sep 23; 9():87. PubMed ID: 18808722
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  • 20. Spectrum and prevalence of mutations from the first 2,500 consecutive unrelated patients referred for the FAMILION long QT syndrome genetic test.
    Kapplinger JD, Tester DJ, Salisbury BA, Carr JL, Harris-Kerr C, Pollevick GD, Wilde AA, Ackerman MJ.
    Heart Rhythm; 2009 Sep 23; 6(9):1297-303. PubMed ID: 19716085
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