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Article

A mutation in CALM1 encoding calmodulin in familial idiopathic ventricular fibrillation in childhood and adolescence.

Journal of the American College of Cardiology - 28 Jan 2014

Marsman Roos F, Barc Julien, Beekman Leander, Alders Marielle, Dooijes Dennis, van den Wijngaard Arthur, Ratbi Ilham, Sefiani Abdelaziz, Bhuiyan Zahurul A, Wilde Arthur A M, Bezzina Connie R

Abstract excerpt

OBJECTIVES: This study aimed to identify the genetic defect in a family with idiopathic ventricular fibrillation (IVF) manifesting in childhood and adolescence. BACKGROUND: Although sudden cardiac death in the young is rare, it frequently presents as the first clinical manifestation of an underlying inherited arrhythmia syndrome. Gene discovery for IVF is important as it enables the identification of individuals...

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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Source

Identifiers

PMID: 24076290
DOI: 10.1016/j.jacc.2013.07.091

Genes

CALM1

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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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