Filamin-A-Related Myxomatous Mitral Valve Dystrophy: Genetic, Echocardiographic and Functional Aspects
A. Lardeux, Vincent Probst(Centre National de la Recherche Scientifique), Florence Kyndt(Inserm), Hervé Le Marec(Centre National de la Recherche Scientifique), Simon Lecointe(Centre National de la Recherche Scientifique), Jean Mérot, Thierry Le Tourneau(Centre National de la Recherche Scientifique), Jean‐Jacques Schott(Centre National de la Recherche Scientifique)
Cited by 48
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