Factor V leiden and prothrombin gene G20210A mutation in children with cerebral thromboembolism
✍ Scribed by Mariana Bonduel; Gabriela Sciuccati; Mirta Hepner; Graciela Pieroni; Aurora Feliú Torres; Claudia Mardaraz; Juan Pablo Frontroth
- Publisher
- John Wiley and Sons
- Year
- 2003
- Tongue
- English
- Weight
- 70 KB
- Volume
- 73
- Category
- Article
- ISSN
- 0361-8609
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📜 SIMILAR VOLUMES
Factor V G1691A (FV-Leiden) and prothrombin (PRT) G20210A single nucleotide polymorphisms (SNPs) were associated with venous thrombosis among Caucasians. We assessed the contribution of both SNPs to the genetic susceptibility of deep venous thrombosis (DVT) among Lebanese and Tunisian patients. Subj
## 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