Characterization of a causative mutation of hemophilia A identified in the promoter region of the factor VIII gene (F8)
Author:
Publisher
Wiley
Subject
Hematology
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1538-7836.2007.02806.x/fullpdf
Reference11 articles.
1. Molecular basis of haemophilia A;Oldenburg;Haemophilia,2004
2. Kemball-Cook G Haemophilia A Mutation Database http://europium.csc.mrc.ac.uk/WebPages/Main/main.htm
3. 2% Haemophilia A patients without mutation in the FVIII gene;Uen;Hamostaseologie,2003
4. Spectrum of molecular defects and mutation detection rate in patients with mild and moderate hemophilia A;Bogdanova;Hum Mutat,2007
5. Role of the liver-enriched transcription factor hepatocyte nuclear factor 1 in transcriptional regulation of the factor VIII gene;McGlynn;Mol Cell Biol,1996
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2. Evidence of pathogenicity of a mutation in 3′ untranslated region causing mild haemophilia A;Haemophilia;2016-05-24
3. Characterization of four novel molecular changes in the promoter region of the factor VIII gene;Haemophilia;2013-12-30
4. Identification and characterization of mutations in the promoter region of the factor VIII gene;Journal of Thrombosis and Haemostasis;2012-02
5. Deep intronic variations may cause mild hemophilia A;Journal of Thrombosis and Haemostasis;2011-08
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