Biallelic variants in POPDC2 cause a novel autosomal recessive syndrome presenting with cardiac conduction defects and variable hypertrophic cardiomyopathy. - Nicastro M; Vermeer AMC; Postema PG; Tadros R; Bowling FZ; Aegisdottir HM; Tragante V; Mach L; Postma AV; Lodder EM; van Duijvenboden K; Zwart R; et al. (MedRxiv : the preprint server for health sciences, 2024)