A single adeno-associated virus (AAV)-murine factor VIII vector partially corrects the hemophilia A phenotype
Author:
Publisher
Wiley
Subject
Hematology
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1046/j.1538-7836.2003.00096.x/fullpdf
Reference43 articles.
1. The molecular basis of hemophilia A in man
2. Expression and Structure-Function Properties of Recombinant Factor VIII
3. A Gene Therapy Approach to Regulated Delivery of Erythropoietin as a Function of Oxygen Tension
4. Regulation of gene expression in vivo following transduction by two separate rAAV vectors
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