Multiple arrhythmic syndromes in a newborn, owing to a novel mutation in SCN5A

Research output: Contribution to journalJournal articleResearchpeer-review

Mutations in the SCN5A gene have been linked to Brugada syndrome (BrS), conduction disease, Long QT syndrome (LQT3), atrial fibrillation (AF), and to pre- and neonatal ventricular arrhythmias.
Original languageEnglish
JournalCanadian Journal of Physiology and Pharmacology
Issue number10
Pages (from-to)723-36
Number of pages14
Publication statusPublished - 2011

    Research areas

  • Animals, Arrhythmias, Cardiac, CHO Cells, Cell Line, Transformed, Cricetinae, DNA Mutational Analysis, Female, Humans, Infant, Newborn, Ion Channels, Membrane Potentials, Mutation, Missense, NAV1.5 Voltage-Gated Sodium Channel, Patch-Clamp Techniques, Sodium Channels, Syndrome

ID: 33964949