[Heterozygous prothrombin gene mutation G20210A and associated diseases].

Granel, B; Morange, P-E; Serratrice, J; Ene, N; Cremades, S; Swiader, L; Disdier, P; Juhan-Vague, I; Weiller, P-J

[Heterozygous prothrombin gene mutation G20210A and associated diseases]. / Mutation G20210A du gène de la prothrombine à l'état hétérozygote et pathologies associées.

Granel, B; Morange, P-E; Serratrice, J; Ene, N; Cremades, S; Swiader, L; Disdier, P; Juhan-Vague, I; Weiller, P-J.

Affiliation

Granel B; Service de médecine interne, centre hospitalier universitaire Timone, 264, rue Saint-Pierre, 13385 Marseille cedex 5, France.

Rev Med Interne ; 24(5): 282-7, 2003 May.

Article in Fr | MEDLINE | ID: mdl-12763173

Subject(s)

Heterozygote; Mutation/genetics; Prothrombin/genetics; Pulmonary Embolism/genetics; Thrombosis/genetics; Adult; Aged; Arteries; Female; France/epidemiology; Genetic Carrier Screening; Genetic Testing/methods; Humans; Male; Middle Aged; Polymerase Chain Reaction; Polymorphism, Genetic/genetics; Prothrombin/metabolism; Pulmonary Embolism/blood; Pulmonary Embolism/epidemiology; Retrospective Studies; Risk Factors; Thrombosis/blood; Thrombosis/epidemiology; Veins

Search on Google

Add to My VHL

XML

PubMed Links

Collection: 01-internacional Database: MEDLINE Main subject: Pulmonary Embolism / Thrombosis / Prothrombin / Heterozygote / Mutation Type of study: Etiology_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Limits: Adult / Aged / Female / Humans / Male / Middle aged Country/Region as subject: Europa Language: Fr Journal: Rev Med Interne Year: 2003 Document type: Article Affiliation country: France Country of publication: France

Search on Google

Add to My VHL

XML

PubMed Links