The genetic basis of inhibitor development in haemophilia A
Author:
Publisher
Wiley
Subject
Genetics (clinical),Hematology,General Medicine
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1046/j.1365-2516.1998.440543.x/fullpdf
Reference7 articles.
1. Absence of inhibitors in previously untreated patients with severe haemophilia A after exposure to a single intermediate purity factor VIII product;Yee;Thromb Haemost,1997
2. Haemophilia A: mutation type determines risk of inhibitor formation;Schwaab;Thromb Haemost,1995
3. Partial correction of a severe molecular defect in hemophilia A, because of errors during expression of the factor VIII gene;Young;Am J Hum Genet,1997
4. Nonsense mutations inhibit RNA splicing in a cell-free system; recognition of mutant codon is independent of protein synthesis;Aoufouchi;Cell,1996
5. Analysis of factor VIII mRNA reveals defects in everyone of 28 haemophilia A patients;Naylor;Hum Mol Genet,1993
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1. Clinical conditions and risk factors for inhibitor‐development in patients with haemophilia: A decade‐long prospective cohort study in Japan, J‐HIS2 (Japan Hemophilia Inhibitor Study 2);Haemophilia;2022-06-11
2. Spectrum of F8 Genotype and Genetic Impact on Inhibitor Development in Patients with Hemophilia A from Multicenter Cohort Studies (J-HIS) in Japan;Thrombosis and Haemostasis;2020-11-30
3. Characterization of a genetically engineered mouse model of hemophilia A with complete deletion of the F8 gene;Journal of Thrombosis and Haemostasis;2016-01-08
4. Blood Clotting Factor VIII: From Evolution to Therapy;Acta Naturae;2013-06-15
5. Mutation spectrum and inhibitor risk in 100 Korean patients with severe haemophilia A;Haemophilia;2012-06-29
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