Antithrombin III Mutation Database: First Update
- 1 January 1993
- journal article
- research article
- Published by Georg Thieme Verlag KG in Thrombosis and Haemostasis
- Vol. 70 (02) , 361-369
- https://doi.org/10.1055/s-0038-1649581
Abstract
No abstract availableThis publication has 30 references indexed in Scilit:
- Identification of nine novel mutations in type I antithrombin deficiency by heteroduplex screeningBritish Journal of Haematology, 1993
- A Recurrent Deletion in the Antithrombin Gene, AT106-108(-6 bp), Identified by DNA Heteroduplex DetectionGenomics, 1993
- Complete nucleotide sequence of the antithrombin gene: Evidence for homologous recombination causing thrombophiliaBiochemistry, 1993
- Screening for mutations in the antithrombin III gene causing recurrent venous thrombosis by single-strand conformation polymorphism analysisHuman Mutation, 1993
- Pleiotropic effects of antithrombin strand 1C substitution mutations.Journal of Clinical Investigation, 1992
- De novo splice site mutation in the antithrombin III (AT3) gene causing recurrent venous thrombosis: Demonstration of exon skipping by ectopic transcript analysisGenomics, 1992
- Novel point mutations leading to type 1 antithrombin deficiency and thrombosisBritish Journal of Haematology, 1991
- Implications of the three-dimensional structure of .alpha.1-antitrypsin for structure and function of serpinsBiochemistry, 1989
- 9 Antithrombin: Structure, genomic organization, function and inherited deficiencyBailliere's Clinical Haematology, 1989
- The site in human antithrombin for functional proteolytic cleavage by human thrombinFEBS Letters, 1981