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Article

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

Annals of medicine - 1 Jan 2004

Laitinen Päivi J, Swan Heikki, Piippo Kirsi, Viitasalo Matti, Toivonen Lauri, Kontula Kimmo

Abstract excerpt

Familial catecholaminergic polymorphic ventricular tachycardia (CPVT) is a rare arrhythmogenic disease manifesting with exercise- or stress-induced ventricular arrhythmias, syncope, and even sudden death. CPVT is inherited as an autosomal dominant or autosomal recessive trait, usually with high penetrance. We characterized in detail the clinical, structural and electrocardiographic findings in this disorder and...

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Share to Catecholamines
Share to Chromosomes, Human, Pair 1

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Death, Sudden, Cardiac

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Share to Polymorphism, Single Nucleotide

Share to Ryanodine Receptor Calcium Release Channel

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Source

Identifiers

PMID: 15176428
DOI: 10.1080/17431380410032599

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-08.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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