Novel Brugada <i>SCN5A</i> Mutation Leading to ST Segment Elevation in the Inferior or the Right Precordial Leads
F Potet, Hervé Le Marec(Centre National de la Recherche Scientifique), Jean‐Jacques Schott(Centre National de la Recherche Scientifique), Philippe Mabo, Jean‐Claude Daubert(Centre Hospitalier Universitaire de Rennes), GUILLAUME LE COQ(Inserm), Gilles Guihard(Inserm), Vincent Probst(Centre National de la Recherche Scientifique), Denis Escande(Institut du Thorax), Fabrice Airaud(Centre Hospitalier Universitaire de Nantes)
Cited by 110
Related Papers
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
Long-Term Prognosis of Patients Diagnosed With Brugada Syndrome
|Circulation|2010|850