Genes, exercise and sudden death: molecular basis of familial catecholaminergic polymorphic ventricular tachycardia

P J Laitinen, H Swan, K Piippo, M Viitasalo, L Toivonen, K Kontula

Research output: Contribution to journalReview ArticleScientificpeer-review

Original languageEnglish
JournalAnnals of Medicine
Volume36
Pages (from-to)81-86
Number of pages6
ISSN0785-3890
DOIs
Publication statusPublished - 2004
MoE publication typeA2 Review article in a scientific journal

Fields of Science

  • arrhythmia
  • catecholaminergic polymorphic ventricular tachycardia
  • gene mutations
  • ryanodine receptor
  • CHANNEL RYANODINE RECEPTOR
  • CA2+ RELEASE CHANNEL
  • CALCIUM-RELEASE
  • CHROMOSOME 1Q42-Q43
  • MUTATIONS
  • ARRHYTHMIAS
  • FKBP12.6
  • DISEASE
  • ARVD2
  • IDENTIFICATION
  • 312 Clinical medicine

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