Conditional ablation of MCU exacerbated cardiac pathology in a genetic arrhythmic model of CPVT
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Background: Catecholaminergic polymorphic ventricular tachycardia (CPVT) is a genetic arrhythmic syndrome caused by mutations in the calcium (Ca2+) release channel ryanodine receptor (RyR2) and its accessory proteins. These mutat... ...
