Factor XI gene mutations in factor XI deficient patients of the Czech Republic
Author:
Publisher
Wiley
Subject
Hematology
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1002/ajh.21286/fullpdf
Reference26 articles.
1. Location of the disulfide bonds in human coagulation factor XI: The presence of tandem apple domains;McMullen;Biochemistry,1991
2. Association of factor XI and high molecular weight kininogen in human plasma;Thompson;J Clin Invest,1977
3. The coagulation cascade: Initiation, maintenance, and regulation;Davie;Biochemistry,1991
4. Factor XI deficiency-from molecular genetics to clinical management;O'Connell;Blood Coagul Fibrinolysis,2003
5. Factor XI Deficiency
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2. Clinical manifestations and mutation spectrum of 57 subjects with congenital factor XI deficiency in China;Blood Cells, Molecules, and Diseases;2016-05
3. A novel c.290G>A mutation in the Factor 11 gene in a Dutch Caucasian family with a Factor XI deficiency;Thrombosis Research;2015-04
4. The spectrum of factor XI deficiency in Italy;Haemophilia;2013-09-24
5. Type I mutation in the F11 gene is a third ancestral mutation which causes factor XI deficiency in Ashkenazi Jews;Journal of Thrombosis and Haemostasis;2013-04
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