Pathophysiology of RyR2 mutation at binding site of FKBP12.6 leading to aberrant opening of the channel in diastole.
Figure adapted from:
• Wleklinski MJ, Kannankeril PJ, Knollmann BC. Molecular and tissue mechanisms of catecholaminergic polymorphic ventricular tachycardia. J Physiol. 2020; 598(14):2817–2834. https://doi.org/10.1113/JP276757
• Tong M, Jiang Y. FK506-Binding Proteins and Their Diverse Functions. Curr Mol Pharmacol. 2015; 9(1):48–65. https://doi.org/10.2174/1874467208666150519113541.