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Article

Factor V Leiden mutation in Turkish patients with homozygous cystathionine beta-synthase deficiency.

Journal of inherited metabolic disease - 1 Jun 2001

Kalkanoğlu H S, Coşkun T, Aydoğdu S D, Tokatli A, Gürgey A

Abstract excerpt

Venous and arterial thromboembolism can occur in patients with homocystinuria. Resistance to activated protein C, which is caused by a single point mutation in the gene for factor V, renders an individual at risk for thrombosis. It has been suggested that coexistence of hereditary homocystinuria and factor V Leiden mutation might jointly play a role in the development of thrombosis. We analysed six patients with...

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Identifiers

PMID: 11486902
DOI: 10.1023/a:1010556603183

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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.

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