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Journal Abstract Search

382 related items for PubMed ID: 24112685

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  • 2. Genetic mutation in Korean patients of sudden cardiac arrest as a surrogating marker of idiopathic ventricular arrhythmia.
    Son MK, Ki CS, Park SJ, Huh J, Kim JS, On YK.
    J Korean Med Sci; 2013 Jul; 28(7):1021-6. PubMed ID: 23853484
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  • 3. 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 Jul; 56(4):450-3. PubMed ID: 26118593
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  • 4. Unexplained drownings and the cardiac channelopathies: a molecular autopsy series.
    Tester DJ, Medeiros-Domingo A, Will ML, Ackerman MJ.
    Mayo Clin Proc; 2011 Oct; 86(10):941-7. PubMed ID: 21964171
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  • 11. Bringing home the bacon? The next step in cardiac sodium channelopathies.
    Wilde AA, Postema PG.
    J Clin Invest; 2015 Jan; 125(1):99-101. PubMed ID: 25500878
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  • 16. 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; 84(2):161-168. PubMed ID: 31696929
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  • 17. A homozygous SCN5A mutation in a severe, recessive type of cardiac conduction disease.
    Neu A, Eiselt M, Paul M, Sauter K, Stallmeyer B, Isbrandt D, Schulze-Bahr E.
    Hum Mutat; 2010 Aug; 31(8):E1609-21. PubMed ID: 20564468
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  • 20. Sudden infant death syndrome-associated mutations in the sodium channel beta subunits.
    Tan BH, Pundi KN, Van Norstrand DW, Valdivia CR, Tester DJ, Medeiros-Domingo A, Makielski JC, Ackerman MJ.
    Heart Rhythm; 2010 Jun; 7(6):771-8. PubMed ID: 20226894
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