Type II antithrombin deficiency caused by a founder mutation Pro73Leu in the Finnish population: clinical picture
Author:
Affiliation:
1. Hemostasis Laboratory; Finnish Red Cross Blood Service; Helsinki Finland
2. Public Health Genomics Unit; Department of Chronic Disease Prevention; National Institute for Health and Welfare; Helsinki Finland
Funder
Finnish Red Cross
Promoting Laboratory Medicine
Research Foundation for Clinical Chemistry
Publisher
Wiley
Subject
Hematology
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/jth.12364/fullpdf
Reference20 articles.
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2. Inherited antithrombin deficiency: a review;Patnaik;Haemophilia,2008
3. The phenotypic and genetic assessment of antithrombin deficiency;Cooper;Int J Lab Hematol,2011
4. Prevalence of antithrombin deficiency in the healthy population;Tait;Br J Haematol,1994
5. Antithrombin mutation database: 2nd (1997) update. For the Plasma Coagulation Inhibitors Subcommittee of the Scientific and Standardization Committee of the International Society on Thrombosis and Haemostasis;Lane;Thromb Haemost,1997
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