Molecular characterization of 11 novel mutations in patients with heterozygous and homozygous FV deficiency
Author:
Publisher
Wiley
Subject
Genetics(clinical),Hematology,General Medicine
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1365-2516.2010.02330.x/fullpdf
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2. Detailed mechanisms of the inactivation of factor VIIIa by activated protein C in the presence of its cofactors, protein S and factor V;Gale;J Biol Chem,2008
3. Rarer quantitative and qualitative abnormalities of coagulation;Girolami;Clin Haematol,1985
4. Parahaemophilia: haemorrhagic diathesis due to absence of previously unknown clotting factor;Owren;Lancet,1947
5. The rare coagulation disorders - review with guidelines for management from the United Kingdom Haemophilia Centre Doctors’ Organisation;Bolton-Maggs;Haemophilia,2004
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2. Hereditary factor V deficiency from heterozygous mutations with a novel variant p.Pro798Leufs∗13 in the F5 gene;Blood Coagulation & Fibrinolysis;2021-06-07
3. Analysis of f5 gene polymorphism in men with coronary atherosclerosis using whole exome sequencing;Атеросклероз;2021-05-03
4. Novel splicing (c.6529-1G>T) and missense (c.1667G>A) mutations causing factor V deficiency;Blood Coagulation & Fibrinolysis;2021-03-23
5. A Comprehensive Overview of Coagulation Factor V and Congenital Factor V Deficiency;Seminars in Thrombosis and Hemostasis;2019-05-23
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