Abstract 17361: Phenotype of the Aortic Valve in Patients With Filamin-A Mutations: Echocardiographic Features and Clinical Outcomes
Romain Capoulade, Thierry Le Tourneau, Guillaume Guimbretière, Toon Omen(St. Antonius Ziekenhuis), Jean‐Jacques Schott(Centre National de la Recherche Scientifique), Daniel Berstein(Stanford Medicine), Jean‐Noël Trochu, Caroline Cueff(Lyon 1 Université), Hervé Le Marec(Centre National de la Recherche Scientifique), Jonathan A Berstein(Stanford Medicine), Claire Toquet(Centre Hospitalier Universitaire de Nantes), Jan J.J. Aalberts(University Medical Center Groningen), Jean Mérot, Nicolas Piriou(Centre Hospitalier Universitaire de Besançon), Stéphanie Blandin(Centre National de la Recherche Scientifique)
Cited by 0
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
Mavacamten for treatment of symptomatic obstructive hypertrophic cardiomyopathy (EXPLORER-HCM): a randomised, double-blind, placebo-controlled, phase 3 trial
|The Lancet|2020|1.2k