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
Author:
Funder
Universidad de Guadalajara, Guadalajara, Jalisco, México
Publisher
Elsevier BV
Subject
Cell Biology,Hematology,Molecular Biology,Molecular Medicine
Reference45 articles.
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3. Are int22h-mediated deletions a common cause of hemophilia?;Abelleyro;Ann. Hematol.,2012
4. Factor VIII gene inversions in severe hemophilia a: results of an international consortium study;Antonarakis;Blood,1995
5. F8 gene mutation type and inhibitor development in patients with severe hemophilia A: systematic review and meta-analysis;Gouw;Blood,2012
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