Introns 1 and 22 inversions and factor VIII inhibitors in patients with severe haemophilia A in southern Brazil
Author:
Publisher
Wiley
Subject
Genetics(clinical),Hematology,General Medicine
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1365-2516.2008.01868.x/fullpdf
Reference47 articles.
1. Inversions disrupting the factor gene are a common cause of severe haemophilia A;Lakich;Nature Genet,1993
2. Haemophilia A: molecular insights;Castaldo;Clin Chem Lab Med,2007
3. F8 gene mutation profile and ITT response in a cohort of Italian haemophilia A patients with inhibitors;Salviato;Haemophilia,2007
4. Factor VIII gene inversions in severe haemophilia A: results of an international consortium study;Antonarakis;Blood,1995
5. Genetic risk factors for inhibitors to factors VIII and IX;Oldenburg;Haemophilia,2006
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1. Investigating the influence of LCT rs3754689 polymorphism on inhibitor development in Iranian and Afghan patients with severe hemophilia A;Blood Coagulation & Fibrinolysis;2020-01
2. Identification of the Intron 22 and Intron 1 Inversions of the Factor VIII Gene in Iraqi Kurdish Patients With Hemophilia A;Clinical and Applied Thrombosis/Hemostasis;2020-01-01
3. Prevalence of factor VIII inhibitors among Afghan patients with hemophilia A;Blood Coagulation & Fibrinolysis;2018-12
4. Genetics of Hypercoagulable and Hypocoagulable States;Neurosurgery Clinics of North America;2018-10
5. F8 inversions of introns 22 and 1 confer a moderate risk of inhibitors in Mexican patients with severe hemophilia A. Concordance analysis and literature review;Blood Cells, Molecules, and Diseases;2018-07
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