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Article

The P-selectin gene polymorphism Val168Met: a novel risk marker for the occurrence of primary ventricular fibrillation during acute myocardial infarction.

Journal of cardiovascular electrophysiology - 1 Nov 2010

Elmas Elif, Bugert Peter, Popp Tatjana, Lang Siegfried, Weiss Christel, Behnes Michael, Borggrefe Martin, Kälsch Thorsten

Abstract excerpt

UNLABELLED: The P-Selectin Gene Polymorphism Val168Met. AIMS: Ventricular fibrillation (VF) in the setting of acute myocardial infarction (AMI) is the leading cause of sudden cardiac death (SCD). Family history of SCD is described as risk factor for primary VF during acute AMI. Genetic factors may be associated with primary VF. We examined polymorphisms in genes related to the activation and adhesion of blood...

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Source

Identifiers

PMID: 20586826
DOI: 10.1111/j.1540-8167.2010.01833.x

Genes

SELP
SCD
SELPLG
ZFHX3

Variants

rs2106261
rs2106261
rs2106261
rs2106261
rs2106261
rs2106261
rs2106261
rs2106261

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-08.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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Semantic proximity does not establish scientific evidence. Graph snapshot: 2026-09-29.

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