Functional characterization of a novel missense mutation identified in a Turkish patient affected by severe coagulation factor V deficiency
Author:
Publisher
Wiley
Subject
Genetics(clinical),Hematology,General Medicine
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1365-2516.2011.02621.x/fullpdf
Reference36 articles.
1. Factor V: a prototype pro-cofactor for vitamin K-dependent enzyme complexes in blood clotting;Jenny;Baillieres Clin Haematol,1989
2. Factor V: a combination of Dr Jekyll and Mr Hyde;Mann;Blood,2003
3. Blood coagulation factors V and VIII: structural and functional similarities and their relationship to hemorrhagic and thrombotic disorders;Kane;Blood,1988
4. Coagulation factors V and VIII and ceruloplasmin constitute a family of structurally related proteins;Church;Proc Natl Acad Sci USA,1984
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2. A Comprehensive Overview of Coagulation Factor V and Congenital Factor V Deficiency;Seminars in Thrombosis and Hemostasis;2019-05-23
3. Functional characterization of a novel missense mutation, His147Arg, in A1 domain of FV protein causing type II deficiency;Thrombosis Research;2014-07
4. Asp68His mutation in the A1 domain of human factor V causes impaired secretion and ineffective translocation;Haemophilia;2014-06-03
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