Molecular basis of type I antithrombin deficiency in two women with recurrent venous thromboembolism in the first trimester of pregnancy
Author:
Publisher
Elsevier BV
Subject
Cell Biology,Hematology,Molecular Biology,Molecular Medicine
Reference20 articles.
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3. Antithrombin Cambridge Ii (A384s): an underestimated genetic risk factor for venous thrombosis;Corral;Blood,2007
4. Homozygous antithrombin deficiency type Ii (99 Leu to Phe mutation) and childhood thromboembolism;Kuhle;Thromb. Haemost.,2001
5. Hereditary and acquired antithrombin deficiency: epidemiology, pathogenesis and treatment options;Maclean;Drugs,2007
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