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Autor:
Xiaolei Pei, Wenwei Shao, Allene Xing, Charles Askew, Xiaojing Chen, Caibin Cui, Yasmina L. Abajas, David A. Gerber, Elizabeth P. Merricks, Timothy C. Nichols, Wuping Li, R. Jude Samulski, Chengwen Li
Publikováno v:
Molecular Therapy: Methods & Clinical Development, Vol 18, Iss , Pp 259-268 (2020)
Adeno-associated virus (AAV) vectors have been successfully used in patients with bleeding disorders and blindness. For human liver targeting, two major factors restrict effective AAV transduction after systemic administration of AAV vectors: human h
Externí odkaz:
https://doaj.org/article/ffd1eccee8e6456aa953cf4176aa8c2d