Contribution of clinically relevant copy number variations in long QT syndrome: a large cohort study
Event: EHRA 2024
Topic: Genetic Aspects of Arrhythmias
Session: Basic science: genetic
FHOD3 is a novel disease causing gene in hypertrophic cardiomyopathy
Event: ESC Congress 2018
Topic: Hypertrophic Cardiomyopathy
Session: Genetics in cardiomyopathies
ESC 365 is supported by
