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Journal Abstract Search

203 related items for PubMed ID: 27460199

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  • 2. Cardiac channelopathy testing in 274 ethnically diverse sudden unexplained deaths.
    Wang D, Shah KR, Um SY, Eng LS, Zhou B, Lin Y, Mitchell AA, Nicaj L, Prinz M, McDonald TV, Sampson BA, Tang Y.
    Forensic Sci Int; 2014 Apr; 237():90-9. PubMed ID: 24631775
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  • 3. Genetic variants in KCNE1, KCNQ1, and NOS1AP in sudden unexplained death during daily activities in Chinese Han population.
    Huang J, Wang X, Hao B, Chen Y, Liu H, Quan L, Tang D, Sheng L, Li M, Huang E, Liu C, Luo B.
    J Forensic Sci; 2015 Mar; 60(2):351-6. PubMed ID: 25639344
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  • 4. 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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  • 9. Common variants in cardiac ion channel genes are associated with sudden cardiac death.
    Albert CM, MacRae CA, Chasman DI, VanDenburgh M, Buring JE, Manson JE, Cook NR, Newton-Cheh C.
    Circ Arrhythm Electrophysiol; 2010 Jun 10; 3(3):222-9. PubMed ID: 20400777
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  • 11. Variant frequencies of KCNQ1, KCNH2, and SCN5A in a Chinese inherited arrhythmia cohort and other disease cohorts undergoing genetic testing.
    Li X, Liu N, Bai R.
    Ann Hum Genet; 2020 Mar 10; 84(2):161-168. PubMed ID: 31696929
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  • 12. [KCNQ1, KCNH2, KCNE1 and KCNE2 potassium channels gene variants in sudden manhood death syndrome].
    Zhao QH, Liu C, Lu LW, Lü GL, Liu H, Tang SB, Quan L, Cheng JD.
    Fa Yi Xue Za Zhi; 2012 Oct 10; 28(5):337-41, 346. PubMed ID: 23213782
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  • 14. Cardiac sodium channel gene variants and sudden cardiac death in women.
    Albert CM, Nam EG, Rimm EB, Jin HW, Hajjar RJ, Hunter DJ, MacRae CA, Ellinor PT.
    Circulation; 2008 Jan 01; 117(1):16-23. PubMed ID: 18071069
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  • 15. Unexplained drownings and the cardiac channelopathies: a molecular autopsy series.
    Tester DJ, Medeiros-Domingo A, Will ML, Ackerman MJ.
    Mayo Clin Proc; 2011 Oct 01; 86(10):941-7. PubMed ID: 21964171
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  • 16. 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 01; 56(4):450-3. PubMed ID: 26118593
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  • 18. 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 01; 9(3):259-65. PubMed ID: 27114410
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  • 19. 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 01; 4(10):1306-14. PubMed ID: 17905336
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