The P303T mutation in the human factor VII (FVII) gene alters the conformational state of the enzyme and causes a severe functional deficiency
Author:
Publisher
Wiley
Subject
Hematology
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1365-2141.2004.05241.x/fullpdf
Reference35 articles.
1. A Thr359 Met mutation in factor VII of a patient with a hereditary deficiency causes defective secretion of the molecule;Arbini;Blood,1996
2. Isolation and characterization of human factor VII. Activation of factor VII by factor Xa;Bajaj;Journal of Biological Chemistry,1981
3. The crystal structure of the complex of blood coagulation factor VIIa with soluble tissue factor;Banner;Nature,1996
4. Monoclonal anti-human factor VII antibodies. Detection in plasma of a second protein antigenically and genetically related to factor VII;Broze;Journal of Clinical Investigation,1985
5. Cell biology of tissue factor, the principal initiator of blood coagulation;Camerer;Thrombosis and Haemostasis,1996
Cited by 4 articles. 订阅此论文施引文献 订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献
1. A novel compound heterozygous variant linked to hematuria in a family with hereditary factor VII deficiency;The Journal of Gene Medicine;2021-12-30
2. Molecular characterization of iranian patients with inherited coagulation factor VII deficiency;Balkan Journal of Medical Genetics;2017-12-01
3. Inherited Coagulation Factor VII and X Deficiencies Associated with Severe Bleeding Diathesis: Molecular Genetics and Pathophysiology;Current Genomics;2005-10-01
4. Erratum;British Journal of Haematology;2005-02
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