Correlations between clinical and physiological consequences of the novel mutation R878C in a highly conserved pore residue in the cardiac Na⁺ channel

Genetic basis and molecular mechanism for idiopathic ventricular fibrillation

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Cardiac Muscle, Cardiomyopathy, Heart Failure +6

SCN5A mutations associated with an inherited cardiac arrhythmia, long QT syndrome

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Long Qt Syndrome, Cardiomyopathy, Genetic Disorder +6

Natural History of Brugada Syndrome

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Molecular mechanism for an inherited cardiac arrhythmia

Paul B. Bennett, Kazuto Yazawa, Naomasa Makita et al. · Nature · 1995 · 967 citations

Cardiac Muscle, Cardiomyopathy, Molecular Physiology +6

A Single Na ⁺ Channel Mutation Causing Both Long-QT and Brugada Syndromes

Connie R. Bezzina, Marieke W. Veldkamp, Maarten P. van den Berg et al. · Circulation Research · 1999 · 637 citations · Full text

Cardiac Muscle, Family Members, Genetics +16