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Familial thrombophilia is an oligogenetic disease: involvement of the prothrombin G20210A, PROC and PROS gene mutations.
Boinot, C; Borgel, D; Kitzis, A; Guicheteau, M; Aiach, M; Alhenc-Gelas, M.
Affiliation
  • Boinot C; Laboratoire d'Hématologie and Laboratoire de Génétique Cellulaire et Moléculaire, CHU La Miletrie, Poitiers, France.
Blood Coagul Fibrinolysis ; 14(2): 191-6, 2003 Feb.
Article in En | MEDLINE | ID: mdl-12632031
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Collection: 01-internacional Database: MEDLINE Main subject: Prothrombin / Protein C / Protein S / Thrombophilia Type of study: Observational_studies / Risk_factors_studies Limits: Adolescent / Adult / Aged / Female / Humans / Male / Middle aged Language: En Journal: Blood Coagul Fibrinolysis Journal subject: ANGIOLOGIA / HEMATOLOGIA Year: 2003 Document type: Article Affiliation country: Francia
Search on Google
Add to My VHL
Print
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PubMed Links

Collection: 01-internacional Database: MEDLINE Main subject: Prothrombin / Protein C / Protein S / Thrombophilia Type of study: Observational_studies / Risk_factors_studies Limits: Adolescent / Adult / Aged / Female / Humans / Male / Middle aged Language: En Journal: Blood Coagul Fibrinolysis Journal subject: ANGIOLOGIA / HEMATOLOGIA Year: 2003 Document type: Article Affiliation country: Francia