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Homozygous G20210A transition in the prothrombin gene associated with severe venous thrombotic disease: two cases in a French family.

Thrombosis and haemostasis - 1 Dec 1998

Zawadzki C, Gaveriaux V, Trillot N, Bauters A, Watel A, Alhenc-Gelas M, Preudhomme C, Jude B

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PMID: 9869179

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Homozygous G20210A transition in the prothrombin gene associated with severe venous thrombotic disease: two cases in a French family.PMID 9869179Read ↗

Homozygous G20210A prothrombin gene mutation without thromboembolic events: a case report.Semantic proximity Read ↗

Double-homozygosity for factor V Leiden and the prothrombin gene G20210A variant in a young patient with idiopathic venous thrombosis.Semantic proximity Read ↗

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A further case of homozygous G20210A prothrombin gene mutation without thromboembolic events.Semantic proximity Read ↗

Heterozygous prothrombin G20210A gene mutation in a patient with livedoid vasculitis.Semantic proximity Read ↗

Homozygous 20210G/A prothrombin gene mutation associated with bilateral iliac vein thrombosis: a case report.Semantic proximity Read ↗

G20210A prothrombin gene mutation in two siblings with cerebral venous thrombosis.Semantic proximity Read ↗

The prothrombin gene variant 20210A in venous and arterial thromboembolism.Semantic proximity Read ↗

Inherited thrombophilia: an update.Semantic proximity Read ↗

Budd-Chiari syndrome in a patient heterozygous for the G20210A mutation of the prothrombin gene.Semantic proximity Read ↗

The prothrombin 20210 G to A variation and thrombosis.Semantic proximity Read ↗

The prothrombin gene G20210A variant in an unselected thromboembolic population. A Belgian prospective clinical study.Semantic proximity Read ↗

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