Multiple arrhythmic syndromes in a newborn, owing to a novel mutation in SCN5A
Research output: Contribution to journal › Journal article › 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.
Original language | English |
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Journal | Canadian Journal of Physiology and Pharmacology |
Volume | 89 |
Issue number | 10 |
Pages (from-to) | 723-36 |
Number of pages | 14 |
ISSN | 0008-4212 |
DOIs | |
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
Research areas
ID: 33964949