A common SCN5A polymorphism modulates the biophysical defects of SCN5A mutations

Genetic basis and molecular mechanism for idiopathic ventricular fibrillation

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

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Prevalence of the Congenital Long-QT 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

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An international compendium of mutations in the SCN5A-encoded cardiac sodium channel in patients referred for Brugada syndrome genetic testing

Jamie D. Kapplinger, David J. Tester, Mariëlle Alders et al. · Heart Rhythm · 2009 · 764 citations

Life Sciences, Cardiology, Genetics +16