Long-term correction of hemophilia B using adenoviral delivery of CRISPR/Cas9
Author:
Funder
NIH
NCI Cancer Center
Publisher
Elsevier BV
Subject
Pharmaceutical Science
Reference78 articles.
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3. Long-term safety and efficacy of factor IX gene therapy in hemophilia B;Nathwani;N. Engl. J. Med.,2014
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5. Gene delivery to the juvenile mouse liver using rAAV2/8 vectors;Cunningham;Mol. Ther.,2008
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