Multiple arrhythmic syndromes in a newborn, owing to a novel mutation in SCN5A
Publikation: Bidrag til tidsskrift › Tidsskriftartikel › Forskning › fagfællebedømt
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.
| Originalsprog | Engelsk |
|---|---|
| Tidsskrift | Canadian Journal of Physiology and Pharmacology |
| Vol/bind | 89 |
| Udgave nummer | 10 |
| Sider (fra-til) | 723-36 |
| Antal sider | 14 |
| ISSN | 0008-4212 |
| DOI | |
| Status | Udgivet - 2011 |
ID: 33964949