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Article

A three-generation family presenting five cases of homozygosity for the 20210 G to A prothrombin variant.

Thrombosis and haemostasis - 1 Nov 1998

Morange P E, Barthet M C, Henry M, Fontanet H, Aillaud M F, Alessi M C, Juhan-Vague I

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Share to Homozygote
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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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PMID: 9843184

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026.

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A three-generation family presenting five cases of homozygosity for the 20210 G to A prothrombin variant.PMID 9843184Read ↗

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Coexistence of three genetic risk factors in a Spanish thrombophilic family: Factor V Leiden, prothrombin 20210 and a new type I antithrombin deficiency.Semantic proximity Read ↗

Superior sagittal sinus thrombosis in a patient heterozygous for the novel 20210 A allele of the prothrombin gene.Semantic proximity Read ↗

Report of a novel kindred with antithrombin heparin-binding site variant (47 Arg to His): demand for an automated progressive antithrombin assay to detect molecular variants with low thrombotic risk.Semantic proximity Read ↗

Reliable genotyping of the G-20210-A mutation of coagulation factor II (prothrombin).Semantic proximity Read ↗

Coinheritance of factor V Leiden (F5 1691A) and prothrombin 20210 A (F2 20210A) in an Austrian family as cause for early onset of venous thromboembolism.Semantic proximity Read ↗

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What is the clinical relevance of the prothrombin G20210A mutation?Semantic proximity Read ↗

Homozygotes for prothrombin gene 20210 A allele in a thrombophilic family without clinical manifestations of venous thromboembolism.Semantic proximity Read ↗

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