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Long QT syndrome type 13 (LQT13) is caused by loss-of-function mutation in the KCNJ5-encoded cardiac G-protein-coupled inward rectifier potassium channel subtype 4 protein. The electrocardiographic (ECG) features of LQT13 are not described yet.To describe for the first time in detail the phenotype-genotype relationship of the ECG and clinical features in patients with LQT13.The 12-lead ECGs, 24-hour...
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