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Article

LMNA Mutation in a Family with a Strong History of Sudden Cardiac Death.

Genes - 19 Jan 2022

Keil Laura, Berisha Filip, Knappe Dorit, Kubisch Christian, Shoukier Moneef, Kirchhof Paulus, Fabritz Larissa, Hellenbroich Yorck, Woitschach Rixa, Magnussen Christina

Abstract excerpt

We report a family with heterozygous deletion of exons 3-6 of the LMNA gene. The main presentation of affected family members was characterized by ventricular and supraventricular arrhythmias, atrioventricular (AV) block and sudden cardiac death (SCD) but also by severe dilative cardiomyopathy (DCM). We report on two siblings, a 36-year-old female and her 40-year-old brother, who suffer from heart failure with...

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Source

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Identifiers

PMID: 35205214
DOI: 10.3390/genes13020169
PMCID: PMC8871815

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-07.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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