The molecular genetics of familial venous thrombosis
- 30 September 1999
- journal article
- review article
- Published by Elsevier BV in Best Practice & Research Clinical Haematology
- Vol. 12 (3), 479-503
- https://doi.org/10.1053/beha.1999.0037
Abstract
No abstract availableKeywords
This publication has 69 references indexed in Scilit:
- Hyperhomocysteinemia and ThrombosisSeminars in Thrombosis and Hemostasis, 1999
- A candidate genetic risk factor for vascular disease: a common mutation in methylenetetrahydrofolate reductaseNature Genetics, 1995
- Antithrombin: The Principal Inhibitor of ThrombinSeminars in Thrombosis and Hemostasis, 1994
- Mutation in blood coagulation factor V associated with resistance to activated protein CNature, 1994
- Antithrombin Budapest 3 An antithrombin variant with reduced heparin affinity resulting from the substitution L99FFEBS Letters, 1992
- Diagnosis and treatment of homozygous protein C deficiency: Report of the working party on homozygous protein C deficiency of the subcommittee on protein C and protein S, international committee on thrombosis and haemostasisThe Journal of Pediatrics, 1989
- New carbohydrate site in mutant antithrombin (7 Ile→Asn) with decreased heparin affinityFEBS Letters, 1988
- Severe protein C deficiency in newborn infantsThe Journal of Pediatrics, 1988
- Recurrent Venous Thromboembolism in Patients with a Partial Deficiency of Protein SNew England Journal of Medicine, 1984
- Homozygous Protein C Deficiency Manifested by Massive Venous Thrombosis in the NewbornNew England Journal of Medicine, 1984