Hereditary deficiency of all vitamin K-dependent procoagulants and anticoagulants
Author:
Publisher
Wiley
Subject
Hematology
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1365-2141.1990.tb07795.x/fullpdf
Reference21 articles.
1. Acquired Vitamin K-Dependent Carboxylation Deficiency in Liver Disease
2. Congenital deficiency of blood clotting factors II, VII, IX, and X
3. A comparison of human prothrombin, factor IX (Christmas factor), factor X (Stuart factor), and protein S
4. Molecular basis of hemophilia B: a defective enzyme due to an unprocessed propeptide is caused by a point mutation in the factor IX precursor.
5. The functional significance of vitamin K action. Difference in phospholipid binding between normal and abnormal prothrombin
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