Acquired, non-amyloid related factor X deficiency: review of the literature
Author:
Publisher
Wiley
Subject
Genetics (clinical),Hematology,General Medicine
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1365-2516.2012.02773.x/fullpdf
Reference50 articles.
1. Pathways in the activation of human coagulation factor X;Mertens;Biochem J,1980
2. The contributions of Ca2+, phospholipids and tissue-factor apoprotein to the activation of human blood-coagulation factor X by activated factor VII;Bom;Biochem J,1990
3. Hypoprothrombinemia: studies of a case of the idiopathic type and the effect of serum administration;Crockett;Blood,1949
4. A new coagulation defect;Telfer;Br J Haematol,1956
5. Stuart clotting defect. I. Segregation of an hereditary hemorrhagic state from the heterogeneous group heretofore called stable factor (SPCA, proconvertin, factor VII) deficiency;Hougie;J Clin Invest,1957
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