Takotsubo cardiomyopathy and congenital long QT syndrome in a patient with a novel duplication in the Per-Arnt-Sim (PAS) domain of hERG1
Keywords: Congenital long QT syndrome; hERG1; KCNH2; Takotsubo cardiomyopathy; Voltage-gated potassium channel; LQTS; long QT syndrome; PAS domain; Per-Arnt-Sim domain; WT; wild type;