Novel point mutations leading to type 1 antithrombin deficiency and thrombosis
Author:
Publisher
Wiley
Subject
Hematology
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1365-2141.1991.tb04456.x/fullpdf
Reference22 articles.
1. Assignment of the human antithromhin III structural gene to chromosome 1q23–25
2. Antithrombin III Utah: proline-407 to leucine mutation in a highly conserved region near the inhibitor reactive site
3. Molecular genetic survey of 16 kindreds with hereditary antithrombin III deficiency
4. Proposed heparin binding site in antithrombin based on arginine 47. A new variant Rouen-II, 47 Arg to Ser.
5. Antithrombin Vicenza, Ala 384 to Pro (GCA to CCA) mutation, transforming the inhibitor into a substrate
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