Prophylactic treatment of severe factor X deficiency with prothrombin complex concentrate
Author:
Publisher
Wiley
Subject
Genetics(clinical),Hematology,General Medicine
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1046/j.1365-2516.2001.00485.x/fullpdf
Reference17 articles.
1. Inherited factor X deficiency: molecular genetics and pathophysiology;Cooper;Thromb Haemost,1997
2. Roberts H Hoffman M et al Practice et al.,
3. The structural gene for human coagulation factor X is located on chromosome 13q34;Scambler;Cytogenet Cell Genet,1985
4. Congenital factor X deficiency: spectrum of bleeding symptoms in 32 Iranian patients;Peyvandi;Br J Haematol,1998
5. Replacement therapy for congenital factor X deficiency;Knight;Transfusion,1985
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