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Journal Abstract Search

380 related items for PubMed ID: 18774102

  • 1. Identification of large gene deletions and duplications in KCNQ1 and KCNH2 in patients with long QT syndrome.
    Eddy CA, MacCormick JM, Chung SK, Crawford JR, Love DR, Rees MI, Skinner JR, Shelling AN.
    Heart Rhythm; 2008 Sep; 5(9):1275-81. PubMed ID: 18774102
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  • 3. Prevalence and spectrum of large deletions or duplications in the major long QT syndrome-susceptibility genes and implications for long QT syndrome genetic testing.
    Tester DJ, Benton AJ, Train L, Deal B, Baudhuin LM, Ackerman MJ.
    Am J Cardiol; 2010 Oct 15; 106(8):1124-8. PubMed ID: 20920651
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  • 7. 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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  • 8. Long QT syndrome caused by a large duplication in the KCNH2 (HERG) gene undetectable by current polymerase chain reaction-based exon-scanning methodologies.
    Koopmann TT, Alders M, Jongbloed RJ, Guerrero S, Mannens MM, Wilde AA, Bezzina CR.
    Heart Rhythm; 2006 Jan 23; 3(1):52-5. PubMed ID: 16399053
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  • 9. 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 23; 4(10):1306-14. PubMed ID: 17905336
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  • 16. Postmortem molecular analysis of KCNQ1, KCNH2, KCNE1 and KCNE2 genes in sudden unexplained nocturnal death syndrome in the Chinese Han population.
    Liu C, Zhao Q, Su T, Tang S, Lv G, Liu H, Quan L, Cheng J.
    Forensic Sci Int; 2013 Sep 10; 231(1-3):82-7. PubMed ID: 23890619
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  • 17. Posthumous diagnosis of long QT syndrome from neonatal screening cards.
    Gladding PA, Evans CA, Crawford J, Chung SK, Vaughan A, Webster D, Neas K, Love DR, Rees MI, Shelling AN, Skinner JR.
    Heart Rhythm; 2010 Apr 10; 7(4):481-6. PubMed ID: 20167303
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  • 18. Compound heterozygosity for mutations Asp611-->Tyr in KCNQ1 and Asp609-->Gly in KCNH2 associated with severe long QT syndrome.
    Yamaguchi M, Shimizu M, Ino H, Terai H, Hayashi K, Kaneda T, Mabuchi H, Sumita R, Oshima T, Hoshi N, Higashida H.
    Clin Sci (Lond); 2005 Feb 10; 108(2):143-50. PubMed ID: 15500450
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  • 19. Utility of treadmill testing in identification and genotype prediction in long-QT syndrome.
    Wong JA, Gula LJ, Klein GJ, Yee R, Skanes AC, Krahn AD.
    Circ Arrhythm Electrophysiol; 2010 Apr 10; 3(2):120-5. PubMed ID: 20071715
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