Filamin A heart valve disease as a genetic cause of inherited bicuspid and tricuspid aortic valve disease
Constance Delwarde(Centre National de la Recherche Scientifique), Romain Capoulade, Solena Le Scouarnec(Institut du Thorax), Jean‐Jacques Schott(Centre National de la Recherche Scientifique), Florence Kyndt(Inserm), Thierry Le Tourneau, Robin Le Ruz(Institut du Thorax), Daniel Bernstein(Stanford University), Jean‐Christian Roussel(St Vincent's Health), Hervé Le Marec(Centre National de la Recherche Scientifique), Claire Toquet(Centre Hospitalier Universitaire de Nantes), Jan J.J. Aalberts(University Medical Center Groningen), Jean Mérot, Jonathan A. Bernstein(Stanford Medicine), Anne‐Sophie Boureau(Nantes Université)
Cited by 8
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