THE MOLECULAR GENETICS OF ANTITHROMBIN DEFICIENCY
- 1 June 1994
- journal article
- review article
- Published by Wiley in British Journal of Haematology
- Vol. 87 (2) , 221-226
- https://doi.org/10.1111/j.1365-2141.1994.tb04902.x
Abstract
No abstract availableKeywords
This publication has 48 references indexed in Scilit:
- Effects of mutations in the hinge region of serpinsBiochemistry, 1993
- A Recurrent Deletion in the Antithrombin Gene, AT106-108(-6 bp), Identified by DNA Heteroduplex DetectionGenomics, 1993
- C1 inhibitor hinge region mutations produce dysfunction by different mechanismsNature Genetics, 1992
- Antithrombin Budapest 3 An antithrombin variant with reduced heparin affinity resulting from the substitution L99FFEBS Letters, 1992
- Crystal structure of uncleaved ovalbumin at 1·95 Å resolutionJournal of Molecular Biology, 1991
- New carbohydrate site in mutant antithrombin (7 Ile→Asn) with decreased heparin affinityFEBS Letters, 1988
- Antithrombin III Utah: proline-407 to leucine mutation in a highly conserved region near the inhibitor reactive siteBiochemistry, 1988
- Absence of Thrombosis in Subjects with Heterozygous Protein C DeficiencyNew England Journal of Medicine, 1987
- Physiological variant of antithrombin‐III lacks carbohydrate sidechain at Asn 135FEBS Letters, 1987
- Relationship between an enhancer element in the human antithrombin III gene and an immunoglobulin light-chain gene enhancerNature, 1985