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Article

Search for cardiac calcium cycling gene mutations in familial ventricular arrhythmias resembling catecholaminergic polymorphic ventricular tachycardia.

BMC medical genetics - 12 Feb 2009

Marjamaa Annukka, Laitinen-Forsblom Päivi, Lahtinen Annukka M, Viitasalo Matti, Toivonen Lauri, Kontula Kimmo, Swan Heikki

Abstract excerpt

BACKGROUND: Catecholaminergic polymorphic ventricular tachycardia (CPVT) is a severe inherited cardiac disorder caused by mutations predominantly in the ryanodine receptor (RyR2) gene. We sought to identify mutations in genes affecting cardiac calcium cycling in patients with CPVT and in less typ...

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Share to Catecholamines
Share to Child, Preschool
Share to Electrocardiography

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Mutation, Missense

Share to Ryanodine Receptor Calcium Release Channel

Share to Tachycardia, Ventricular

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Source

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Identifiers

PMID: 19216760
DOI: 10.1186/1471-2350-10-12
PMCID: PMC2667497

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 2 Sept 2026. Prepared record publication-19216760-2026-09-02.2. Manifest publication-graph-cohort-2026-09-02.2.

Source receipt: PubMed via Helena Literature Corpus, retrieved 2 Sept 2026.

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