Gene therapy for hemophilia
Author:
Publisher
Elsevier
Reference92 articles.
1. Generation and characterization of E1/E2a/E3/E4‐deficient adenoviral vectors encoding human factor VIII;Andrews;Mol. Ther.,2001
2. Sustained correction of hemophilia B phenotype following intravascular delivery of AAV vector to skeletal muscle;Arruda;Mol. Ther.,2002
3. Sustained high‐level expression of full‐length human factor VIII and restoration of clotting activity in hemophilic mice using a minimal adenovirus vector;Balague;Blood,2000
4. Targeted disruption of the mouse factor VIII gene produces a model of haemophilia A;Bi;Nat. Genet.,1995
5. Further characterization of factor VIII‐deficient mice created by gene targeting: RNA and protein studies;Bi;Blood,1996
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