Identification of a KCNQ1 Polymorphism Acting as a Protective Modifier against Arrhythmic Risk in Long QT Syndrome

BACKGROUND: Long-QT Syndrome (LQTS) is characterized by such striking clinical heterogeneity, that even among family members carrying the same mutation, clinical outcome can range between sudden death to no symptoms. We investigated the role of genetic variants as modifiers of risk for cardiac event...

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Main Authors: Duchatelet, Sabine, Crotti, Lia, Peat, Rachel A., Denjoy, Isabelle, Itoh, Hideki, Berthet, Myriam, Ohno, Seiko, Fressart, Véronique, Monti, Maria Cristina, Crocamo, Cristina, Pedrazzini, Matteo, Dagradi, Federica, Vicentini, Alessandro, Klug, Didier, Brink, Paul A., Goosen, Althea, Swan, Heikki, Toivonen, Lauri, Lahtinen, Annukka M., Kontula, Kimmo, Shimizu, Wataru, Horie, Minoru, George, Alfred L., Trégouët, David-Alexandre, Guicheney, Pascale, Schwartz, Peter J.
Formato: Artigo
Idioma:Inglês
Publicado em: 2013
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Article
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC3864834/
https://ncbi.nlm.nih.gov/pubmed/23856471
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1161/CIRCGENETICS.113.000023
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