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Fibrinolysis in patients with the 1691 G→A mutation in factor V gene and history of deep vein thrombosis

✍ Scribed by M. Stegnar; P. Peternel; P. Uhrin; T. Cvelbar-Marinko; K. Goršič-Tomažic; B.R. Binder

Book ID: 117439322
Publisher: Elsevier Science
Year: 1997
Tongue: English
Weight: 904 KB
Volume: 11
Category: Article
ISSN: 0268-9499
DOI: 10.1016/s0268-9499(97)80051-3

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## Objective: To evaluate the frequency and type of vascular lesions and to study the association of factor v gene g1691a (leiden) and prothrombin gene g20210a polymorphisms with venous thrombosis in italian patients with behçet's disease (bd). ## Methods: Included were 118 consecutive italian bd