/f/125658/7246x3240/f72d1f6fc5/esc-logo-lock-up-red-pos-rgb.png){kind=logo}
Syndromic cardiac disorder is associated with a non-coding deletion that induces a 3D chromatin remodeling and PITX2 expression dysregulation
Event: ESC Congress 2022
Topic: Genetics, Epigenetics, ncRNA
Session: Role of epigenetics in cardiac health and disease
Molecular mechanism of a new cardiac syndrome associated with a regulatory element deletion of chromosome 4q25
Event: ESC Congress 2020
Topic: Genetic Aspects of Arrhythmias
Session: Risk of Sudden Cardiac Death in Patient with Ion Channel Disorders
ESC 365 is supported by
