Familial Catecholamine-Induced QT Prolongation in Unexplained Sudden Cardiac Death

François Huchet(Centre National de la Recherche Scientifique), Jean‐Baptiste Gourraud(Centre Hospitalier Universitaire de Nantes), Julien Barc(Centre National de la Recherche Scientifique), Aurélie Thollet(Institut du Thorax), Flavien Charpentier(Inserm), Florence Kyndt(Inserm), Richard Redon(Centre National de la Recherche Scientifique), Hervé Le Marec(Centre National de la Recherche Scientifique), Jean‐Jacques Schott(Centre National de la Recherche Scientifique), Vincent Probst(Centre National de la Recherche Scientifique)
Journal of the American College of Cardiology
March 1, 2017
10.1016/j.jacc.2017.01.030
Cited by 8

Related Papers

Origins and functional impact of copy number variation in the human genome
|Nature|2009|2k
HRS/EHRA Expert Consensus Statement on the State of Genetic Testing for the Channelopathies and Cardiomyopathies
|Heart Rhythm|2011|1.5k
Congenital Heart Disease Caused by Mutations in the Transcription Factor <i>NKX2-5</i>
|Science|1998|1.3k
Ankyrin-B mutation causes type 4 long-QT cardiac arrhythmia and sudden cardiac death
|Nature|2003|961
HRS/EHRA Expert Consensus Statement on the State of Genetic Testing for the Channelopathies and Cardiomyopathies: This document was developed as a partnership between the Heart Rhythm Society (HRS) and the European Heart Rhythm Association (EHRA)
|EP Europace|2011|904