Multiple arrhythmic syndromes in a newborn, owing to a novel mutation in SCN5A
Research output: Contribution to journal › Journal article › Research › peer-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.
|Journal||Canadian Journal of Physiology and Pharmacology|
|Number of pages||14|
|Publication status||Published - 2011|
- 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