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Article

Expanding the phenotype of sudden cardiac death-An unusual presentation of a family with a Lamin A/C mutation.

International journal of cardiology - 7 Jan 2010

De Backer Julie, Van Beeumen Katarina, Loeys Bart, Duytschaever Mattias

Abstract excerpt

Familial occurrence of sudden cardiac death (SCD) is related to a variety of clinical conditions, which can be delineated in up to 40% of families through a combination of cardiovascular examination and genetic studies. Patients with Lamin A/C gene mutations are at increased risk for SCD, but "laminopathies" are not included into clinical algorithms of SCD. Here we present a family with SCD in the absence of left...

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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Source

Identifiers

PMID: 18691775
DOI: 10.1016/j.ijcard.2008.06.008

Genes

SCD

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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