Intron 22 factor VIII gene inversions in Argentine families with severe haemophilia A
Author:
Publisher
Wiley
Subject
Genetics(clinical),Hematology,General Medicine
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1046/j.1365-2516.2000.00365.x/fullpdf
Reference10 articles.
1. Characterization of the human factor VIII gene;Gitschier;Nature,1984
2. Inversions disrupting the factor VIII gene are common cause of severe haemophilia A;Lakich;Nature Genet,1993
3. Characteristic mRNA abnormality found in half of patients with severe haemophilia A is due to large inversions;Naylor;Hum Mol Genet,1993
4. Investigation of the factor VIII intron 22 repeated region (int22h) and the associated inversion junctions;Naylor;Hum Mol Genet,1995
5. mutation type determines risk of inhibitor formation;Schwaab;Thromb Haemost,1995
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