Pei, J; Schuldt, M; Nagyova, E; Gu, Z; El Bouhaddani, S; Yiangou, L; Jansen, M; Calis, J J A; Dorsch, L M; Blok, C Snijders; van den Dungen, N A M; Lansu, N; Boukens, B J; Efimov, I R; Michels, M; Verhaar, M C; de Weger, R; Vink, A; van Steenbeek, F G; Baas, A F; Davis, R P; Uh, H W; Kuster, D W D; Cheng, C; Mokry, M; van der Velden, J; Asselbergs, F W; Harakalova, M
(Springer-Verlag, 2021-12)
BACKGROUND: Hypertrophic cardiomyopathy (HCM) is the most common genetic disease of the cardiac muscle, frequently caused by mutations in MYBPC3. However, little is known about the upstream pathways and key regulators ...