Bone marrow mesenchymal cells for haemophilia A gene therapy using retroviral vectors with modified long-terminal repeats
Author:
Publisher
Wiley
Subject
Genetics (clinical),Hematology,General Medicine
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1046/j.1365-2516.2003.00709.x/fullpdf
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3. Generation and characterization of e1/e2a/e3/e4-deficient adenoviral vectors encoding human factor VIII;Andrews;Mol Ther,2001
4. 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
5. Development and application of a minimal-adenoviral vector system for gene therapy of hemophilia A;Zhang;Thromb Haemost,1999
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