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Nationwide experience of catecholaminergic polymorphic ventricular tachycardia caused by RyR2 mutations.

Heart (British Cardiac Society) - 1 Jun 2017

Broendberg Anders Krogh, Nielsen Jens Cosedis, Bjerre Jesper, Pedersen Lisbeth Noerum, Kristensen Jens, Henriksen Finn Lund, Bundgaard Henning, Jensen Henrik Kjaerulf

Abstract excerpt

OBJECTIVE: The aim of this study was to characterise disease penetrance, course of disease and use of antiarrhythmic medication and implantable cardioverter-defibrillator (ICD) therapy in a Danish nationwide cohort of patients with catecholaminergic polymorphic ventricular tachycardia (CPVT) due to mutations in the ryanodine receptor-2 (RyR2) gene. METHODS: The study population was identified through the national...

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Identifiers

PMID: 28237968
DOI: 10.1136/heartjnl-2016-310509

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SCD

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 6 Sept 2026. Manifest publication-graph-cohort-2026-09-06.1.

Source receipt: pubmed, retrieved 6 Sept 2026.

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