Gain-of-Function Mutation of the SCN5A Gene Causes Exercise-Induced Polymorphic Ventricular Arrhythmias

Heikki Swan, Mohamed Yassine Amarouch, Jaakko Leinonen, Annukka Marjamaa, Jan P. Kucera, Päivi J. Laitinen-Forsblom, Annukka M. Lahtinen, Aarno Palotie, Kimmo Kontula, Lauri Toivonen, Hugues Abriel, Elisabeth Widen

Research output: Contribution to journalArticleScientificpeer-review

Original languageEnglish
JournalCirculation. Cardiovascular genetics
Volume7
Issue number6
Pages (from-to)771-U111
Number of pages17
ISSN1942-325X
DOIs
Publication statusPublished - Dec 2014
MoE publication typeA1 Journal article-refereed

Fields of Science

  • arrhythmia (heart rhythm disorders)
  • catecholaminergic polymorphic ventricular tachycardia
  • exercise test
  • genetic testing
  • mutation
  • SCN5A
  • LONG QT SYNDROME
  • CARDIAC SODIUM-CHANNEL
  • BRUGADA-SYNDROME
  • CA2+ SPARK
  • IN-VITRO
  • TACHYCARDIA
  • MODEL
  • DISEASE
  • FAMILY
  • ERYTHROMELALGIA
  • 3121 Internal medicine

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