Generation of clinical grade recombinant adeno-associated virus
Recombinant adeno-associated viruses (rAAV) remain one of the most encouraging gene therapy vectors for treating patients with genetic abnormalities. rAAV can safely deliver long-lasting expression of a therapeutic transgene to a wide range of cell types. One challenge with therapeutic rAAV is the...
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Language: | en_US |
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2018
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Online Access: | https://hdl.handle.net/2144/31279 |