Mechanism underlying factor VII deficiency in Jewish populations with the Ala244 Val mutation
Author:
Publisher
Wiley
Subject
Hematology
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1046/j.1365-2141.1999.01436.x/fullpdf
Reference33 articles.
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2. A Thr359Met mutation in factor VII of a patient with a hereditary deficiency causes defective secretion of the molecule;Arbini;Blood,1996
3. Severe factor VII deficiency due to a mutation disrupting a hepatocyte nuclear factor 4 binding site in the factor VII promoter;Arbini;Blood,1996
4. Factor IX is activated in vivo by the tissue factor mechanism;Bauer;Blood,1990
5. Mutation pattern in clinically asymptomatic coagulation factor VII deficiency;Bernardi;Human Mutation,1996
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1. Use of recombinant factor VII for tooth extractions in a patient with severe congenital factor VII deficiency;The Journal of the American Dental Association;2015-04
2. Factor VII Deficiency Resulting in Acute Hemorrhage in Orthognathic Surgery: A Case Report;Journal of Oral and Maxillofacial Surgery;2012-01
3. Characterization of mutations causing factor VII deficiency in 61 unrelated Israeli patients;Journal of Thrombosis and Haemostasis;2004-10
4. Human factor VII deficiency caused by S339C mutation located adjacent to the specificity pocket of the catalytic domain;Clinical & Laboratory Haematology;2002-08
5. Isolated Factor VII Deficiency Diagnosed after a Life-Threatening Brain Haemorrhage;Journal of International Medical Research;2000-12
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