Gene therapy for hemophilia: are viral vectors really feasible?
- PMID: 12871491
- DOI: 10.1046/j.1538-7836.2003.00095.x
Gene therapy for hemophilia: are viral vectors really feasible?
Comment in
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A single adeno-associated virus (AAV)-murine factor VIII vector partially corrects the hemophilia A phenotype.J Thromb Haemost. 2003 Feb;1(2):220-6. doi: 10.1046/j.1538-7836.2003.00096.x. J Thromb Haemost. 2003. PMID: 12871492
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