Factor VIII genotype and inhibitor development in patients with haemophilia A: highest risk in patients with splice site mutations
Author:
Publisher
Wiley
Subject
Genetics (clinical),Hematology,General Medicine
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1365-2516.2008.01694.x/fullpdf
Reference20 articles.
1. The epidemiology of inhibitors in haemophilia A: a systematic review;Wight;Haemophilia,2003
2. Inhibitors in congenital coagulation disorders;Key;Br J Haematol,2004
3. Inhibitors: resolving diagnostic and therapeutic dilemmas;Dimichele;Haemophilia,2002
4. The Malmo International Brother Study (MIBS): further support for genetic predisposition to inhibitor development in hemophilia patients;Astermark;Haemophilia,2001
5. The role of genetics in inhibitor formation;Gill;Thromb Haemost,1999
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2. Race, ethnicity, F8 variants, and inhibitor risk: analysis of the “My Life Our Future” hemophilia A database;Journal of Thrombosis and Haemostasis;2023-04
3. Mutation detection and inhibitor risk in Iranian patients with Hemophilia A: Six novel mutations;Clinical Case Reports;2020-09-15
4. Nonsevere hemophilia A: often overlooked, but not forgotten;Current Opinion in Hematology;2020-07-21
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