Toward gene therapy for hemophilia A with novel adenoviral vectors: successes and limitations in canine models
Author:
Publisher
Wiley
Subject
Hematology
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1538-7836.2006.01964.x/fullpdf
Reference16 articles.
1. GENE THERAPY: Twenty-First Century Medicine
2. Improvements in adenoviral vector technology: overcoming barriers for gene therapy
3. Germline alteration by gene therapy: assessing and reducing the risks
4. Fatal systemic inflammatory response syndrome in a ornithine transcarbamylase deficient patient following adenoviral gene transfer
5. Expanded-capacity adenoviral vectors—the helper-dependent vectors
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