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Autor:
Darrick L. Yu, Laura P. van Lieshout, Brenna A. Y. Stevens, Kelsie J. (Jagt) Near, Jenny K. Stodola, Kevin J. Stinson, Durda Slavic, Sarah K. Wootton
Publikováno v:
Viruses, Vol 16, Iss 1, p 57 (2023)
Adeno-associated virus (AAV) vectors are among the most widely used delivery vehicles for in vivo gene therapy as they mediate robust and sustained transgene expression with limited toxicity. However, a significant impediment to the broad clinical su
Externí odkaz:
https://doaj.org/article/03d782a89b9b4b69b161f7c5f155a7d8