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Article

Prevalence of factor V gene mutation amongst myocardial infarction patients and healthy controls is higher in Sweden than in other countries.

Journal of internal medicine - 1 Mar 1996

Holm J, Zöller B, Berntorp E, Erhardt L, Dahlbäck B

Abstract excerpt

OBJECTIVE: Haemostatic imbalance may be an aetiological factor in the development of acute coronary syndromes. Inherited resistance to activated protein C (APC) is a common disorder associated with hypercoagulability and lifelong risk of venous thrombosis. APC resistance is due to a single mutation in the gene coding for coagulation factor V (FV:Q506). To test the importance of the FV:Q506 mutation in premature...

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Source

Identifiers

PMID: 8772620
DOI: 10.1046/j.1365-2796.1996.470808000.x

Genes

APC

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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.

Related research

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Prevalence of factor V gene mutation amongst myocardial infarction patients and healthy controls is higher in Sweden than in other countries.PMID 8772620Read ↗

Factor V Q506 (resistance to activated protein C) and prognosis after acute coronary syndrome.Semantic proximity Read ↗

Mutation in the gene coding for coagulation factor V and the risk of myocardial infarction, stroke, and venous thrombosis in apparently healthy men.Semantic proximity Read ↗

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Factor V Leiden (resistance to activated protein C) increases the risk of myocardial infarction in young women.Semantic proximity Read ↗

The association of factor V Leiden with myocardial infarction is replicated in 1880 patients with premature disease.Semantic proximity Read ↗

Resistance to activated protein C, the FV:Q506 allele, and venous thrombosis.Semantic proximity Read ↗

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Increased prevalence of the G20210A prothrombin gene variant in acute coronary syndromes without metabolic or acquired risk factors or with limited extent of disease.Semantic proximity Read ↗

Resistance to activated protein C caused by the R506Q mutation in the gene for factor V is a common risk factor for venous thrombosis.Semantic proximity Read ↗

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