Impact of SERPINC1 mutation on thrombotic phenotype in children with congenital antithrombin deficiency—first analysis of the International Society on Thrombosis and Haemostasis pediatric antithrombin deficiency database and biorepository
Author:
Funder
International Society on Thrombosis and Haemostasis Inc
Publisher
Elsevier BV
Subject
Hematology
Reference59 articles.
1. Clinical presentation and molecular basis of congenital antithrombin deficiency in children: a cohort study;Kumar;Br J Haematol,2014
2. Prevalence of antithrombin deficiency in the healthy population;Tait;Br J Haematol,1994
3. Prevalence of antithrombin deficiency in healthy blood donors: a cross-sectional study;Wells;Am J Hematol,1994
4. Clinical and laboratory characteristics of paediatric and adolescent index cases with venous thromboembolism and antithrombin deficiency. An observational multicentre cohort study;Limperger;Thromb Haemost,2014
5. Thrombophilia: common questions on laboratory assessment and management;Heit;Hematology Am Soc Hematol Educ Program,2007
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