Molecular genetics of inherited antithrombin III deficiencies
- 1 September 1989
- journal article
- review article
- Published by Elsevier in The American Journal of Medicine
- Vol. 87 (3) , S15-S18
- https://doi.org/10.1016/0002-9343(89)80525-x
Abstract
No abstract availableKeywords
This publication has 10 references indexed in Scilit:
- Antithrombin-III-Hamilton: a gene with a point mutation (guanine to adenine) in codon 382 causing impaired serine protease reactivityBlood, 1988
- Molecular genetic survey of 16 kindreds with hereditary antithrombin III deficiencyBlood, 1987
- Heparin binding defect in a new antithrombin III variant: Rouen, 47 Arg to HisBlood, 1987
- Antithrombin III Tours gene: Identification of a point mutation leading to an arginine—cysteine replacement in a silent deficiencyNucleic Acids Research, 1986
- Abnormal antithrombin III with defective serine protease binding (antithrombin III "Denver").Journal of Clinical Investigation, 1986
- Enzymatic Amplification of β-Globin Genomic Sequences and Restriction Site Analysis for Diagnosis of Sickle Cell AnemiaScience, 1985
- Molecular Heterogeneity of Inherited Antithrombin III DeficiencyNew England Journal of Medicine, 1983
- Characterization of an unusual DNA length polymorphism 5' to the human antithrombin III geneNucleic Acids Research, 1983
- Cloning and expression of the cDNA for human antithrom, bin IIINucleic Acids Research, 1982
- Actions and Interactions of Antithrombin and HeparinNew England Journal of Medicine, 1975