Associated Papers
Mutational spectrum of congenital long QT syndrome in Turkey; identification of 12 novel mutations across KCNQ1, KCNH2, SCN5A, KCNJ2, CACNA1C, and CALM1.
Akgun-Dogan O et al.
Journal of Cardiovascular Electrophysiology, 2022
Diagnosis and long-term follow-up of the Brugada syndrome in patients with idiopathic ventricular fibrillation.
Remme CA et al.
European Heart Journal, 2001
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