RYR2 gene exon 3 deletion as a cause of convergent polymorphic catecholaminergic ventricular tachycardia and cardiomyopathy characterized by LV systolic dysfunction.
Event: ESC Congress 2024
Topic: Clinical
Session: Monogenetic cardiac diseases
Risk prediction of advanced heart failure in arrhythmogenic cardiomyopathy
Event: Heart Failure 2022
Topic: Epidemiology, Prognosis, Outcome
Session: Heart failure patient profile and outcome 1
