Resistance to activated protein C due to a factor V gene mutation: The most common inherited risk factor of thrombosis
- 29 February 1996
- journal article
- review article
- Published by Elsevier in Trends in Cardiovascular Medicine
- Vol. 6 (2), 45-53
- https://doi.org/10.1016/1050-1738(95)00130-1
Abstract
No abstract availableKeywords
This publication has 52 references indexed in Scilit:
- Population differences in the frequency of the factor V Leiden variant among people with clinically symptomatic protein C deficiency.Journal of Medical Genetics, 1995
- Factor V Leiden Gene Mutation and Thrombin Generation in Relation to the Development of Acute StrokeArteriosclerosis, Thrombosis, and Vascular Biology, 1995
- Factor V Leiden and ThrombophiliaNew England Journal of Medicine, 1995
- Identification of the same factor V gene mutation in 47 out of 50 thrombosis-prone families with inherited resistance to activated protein C.Journal of Clinical Investigation, 1994
- Mutation in blood coagulation factor V associated with resistance to activated protein CNature, 1994
- The molecular basis of blood coagulationCell, 1988
- Absence of Thrombosis in Subjects with Heterozygous Protein C DeficiencyNew England Journal of Medicine, 1987
- 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
- Venous Thromboembolism and Other Venous Disease in the Tecumseh Community Health StudyCirculation, 1973