Haemophilia A mutations in the UK: results of screening one-third of the population
Author:
Publisher
Wiley
Subject
Hematology
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1365-2141.2008.07310.x/fullpdf
Reference38 articles.
1. Factor VIII gene inversions in severe hemophilia A: results of an international consortium study;Antonarakis;Blood,1995
2. Creation of a novel donor splice site in intron 1 of the factor VIII gene leads to activation of a 191 bp cryptic exon in two haemophilia A patients;Bagnall;British Journal of Haematology,1999
3. Recurrent inversion breaking intron 1 of the factor VIII gene is a frequent cause of severe hemophilia A;Bagnall;Blood,2002
4. Inversions causing hemophilia A: novel insight into their origin and a new more discriminant PCR test for their detection;Bagnall;Journal of Thrombosis and Haemostasis,2006
5. Polymorphism and hemophilia A causing inversions in distal Xq28: a complex picture;Bagnall;Journal of Thrombosis and Haemostasis,2006
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