Study of a protein S gene polymorphism at DNA and mRNA level in a family with symptomatic protein S deficiency
- 1 September 1993
- journal article
- case report
- Published by Wiley in British Journal of Haematology
- Vol. 85 (1), 173-175
- https://doi.org/10.1111/j.1365-2141.1993.tb08662.x
Abstract
No abstract availableThis publication has 10 references indexed in Scilit:
- Protein S activity in patients with heredofamilial protein S deficiency and in patients with juvenile venous thrombosis. Results of a functional methodThrombosis Research, 1991
- A CCA/CCG neutral dimorphism in the codon for Pro 626 of the human protein S gene PSα (PROS1)Nucleic Acids Research, 1991
- Organization of the human protein S genesBiochemistry, 1990
- Heerlen polymorphism of protein S, an immunologic polymorphism due to dimorphism of residue 460Blood, 1990
- Partial protein S gene deletion in a family with hereditary thrombophiliaBlood, 1989
- The Regulation of Natural Anticoagulant PathwaysScience, 1987
- Isolation and sequence of the cDNA for human protein S, a regulator of blood coagulation.Proceedings of the National Academy of Sciences, 1986
- Familial protein S deficiency is associated with recurrent thrombosis.Journal of Clinical Investigation, 1984
- Plasma protein S deficiency in familial thrombotic diseaseBlood, 1984
- Characterization of protein S, a .gamma.-carboxyglutamic acid containing protein from bovine and human plasmaBiochemistry, 1979