Experience of immune tolerance in a carrier of severe haemophilia A with inhibitor development post-surgery
Author:
Affiliation:
1. Arthur Bloom Haemophilia Centre; University Hospital Wales; Cardiff UK
2. Haemophilia Centre; Singleton Hospital; Swansea Swansea UK
3. Cardiff University; Cardiff UK
Publisher
Wiley
Subject
Genetics(clinical),Hematology,General Medicine
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/hae.13216/fullpdf
Reference8 articles.
1. Treatment-related risk factors of inhibitor development in previously untreated patients with Haemophilia A: the CANAL Cohort Study;Gouw;Blood,2007
2. Factor VIII gene (F8) mutation and the risk of inhibitor development in non-severe Haemophilia A;Eckhardt;Blood,2013
3. Genetic control of X inactivation and processes leading to X-inactivation skewing;Belmont;Am J Hum Genet,1996
4. Diagnosis and treatment of Factor VIII and IX inhibitors in congenital Haemophilia;Collins;Br J Haematol,2012
5. F8 gene mutation type and inhibitor development in patients with severe Haemophilia A: a systematic review and meta-analysis;Gouw;Blood,2012
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