A novel F11 mutation in a Chinese paediatric patient with severe factor XI deficiency
Author:
Publisher
Elsevier BV
Subject
Hematology
Reference10 articles.
1. Berber, E. Molecular characterization of FXI deficiency. Clin. Appl. Thromb. Hemost., 27–32.
2. The prevalence of hemophilia in mainland China: a systematic review and meta-analysis;Qu;Southeast Asian J Trop Med Public Health,2014
3. Berliner S, Horowitz I, Martinowitz U, et al. Dental surgery in patients with severe factor XI deficiency without plasma replacement. Blood Coagul. Fibrinolysis. 1992;3(4):465–8.
4. Coagulation factor activity and clinical bleeding severity in rare bleeding disorders: results from the European Network of Rare Bleeding Disorders;Peyvandi;J. Thromb. Haemost.,2012
5. An illustrative case and a review on the dosing of recombinant factor VIIa in congenital factor XI deficiency;Schulman;Haemophilia.,2006
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