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- W2034974686 abstract "Congenital long QT syndrome (LQTS) is a heterogeneous group of primary and secondary cardiac channelopathies characterized by delayed myocardial repolarization, QT prolongation, and increased risk of sudden death. Eleven LQTS-susceptibility genes have been discovered so far. Mutations in three cardiac channel α-subunit encoding genes account for approximately 75% of LQTS cases, with KCNQ1-mediated long QT syndrome type 1 (LQT1) representing the most common LQTS subtype. 1 Ackerman M.J. Cardiac channelopathies: it’s in the genes. Nat Med. 2004; 10: 463-464 Crossref PubMed Scopus (138) Google Scholar , 2 Tester D.J. Will M.L. Haglund C.M. et al. Effect of clinical phenotype on yield of long QT syndrome genetic testing. J Am Coll Cardiol. 2006; 47: 764-768 Abstract Full Text Full Text PDF PubMed Scopus (154) Google Scholar" @default.
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- W2034974686 date "2008-03-01" @default.
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- W2034974686 title "Suppression of atrial fibrillation with mexiletine pharmacotherapy in a young woman with type 1 long QT syndrome" @default.
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- W2034974686 doi "https://doi.org/10.1016/j.hrthm.2007.10.029" @default.
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