The molecular basis of haemophilia A
Author:
Publisher
Wiley
Subject
Genetics(clinical),Hematology,General Medicine
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1046/j.1365-2516.1998.440346.x/fullpdf
Reference21 articles.
1. A transcribed gene in an intron of the human factor VIII gene;Levinson;Genomics,1990
2. Evidence for a thrid transcript from the human factor VIII gene;Levinson;Genomics,1992
3. Characterization of type 2N von Willebrand disease using phenotypic and molecular techniques;Nesbitt;Thromb Haemost,1996
4. Structure of human factor VIII;Vehar;Nature,1984
5. Recombinant, B-domain deleted factor VIII (r-VIII SQ): Pharmacokinetics and initial safety aspects in hemophilia A patients;Fijnvandraat;Thromb Haemost,1997
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1. Promising coagulation factor VIII bypassing strategies for patients with haemophilia A;Blood Coagulation & Fibrinolysis;2014-09
2. Hémophilie : physiopathologie et bases moléculaires;EMC - Hématologie;2008-01
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4. Restricted BV gene usage by factor VIII-reactive CD4+ T cells in inhibitor-positive patients with severe hemophilia A;Thrombosis and Haemostasis;2003
5. Adenovirus-Mediated Factor VIII Gene Expression Results in Attenuated Anti-Factor VIII-Specific Immunity in Hemophilia A Mice Compared with Factor VIII Protein Infusion;Human Gene Therapy;2001-09
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