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 |
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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