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Journal Abstract Search

148 related items for PubMed ID: 29851656

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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; 56(4):450-3. PubMed ID: 26118593
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  • 4. Mutation analysis for the detection of long QT-syndrome (LQTS) associated SNPs.
    J E, T D, M S, M KN, J D, M NW.
    Int J Legal Med; 2017 Mar; 131(2):333-338. PubMed ID: 27613431
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  • 7. Genetic Variants on SCN5A, KCNQ1, and KCNH2 in Patients with Ventricular Arrhythmias during Acute Myocardial Infarction in a Chinese Population.
    Wang F, Liu Y, Liao H, Xue Y, Zhan X, Fang X, Liang Y, Wei W, Rao F, Zhang Q, Deng H, Lin Y, Liu F, Lin W, Zhang B, Wu S.
    Cardiology; 2020 Mar; 145(1):38-45. PubMed ID: 31751991
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  • 8. 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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  • 16. Mutations in the SCN5A gene: evidence for a link between long QT syndrome and sudden death?
    Kiehne N, Kauferstein S.
    Forensic Sci Int Genet; 2007 Jun 10; 1(2):170-4. PubMed ID: 19083750
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  • 20. Influence of genetic modifiers on sudden cardiac death cases.
    Jenewein T, Neumann T, Erkapic D, Kuniss M, Verhoff MA, Thiel G, Kauferstein S.
    Int J Legal Med; 2018 Mar 10; 132(2):379-385. PubMed ID: 29214556
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