Circumventing the packaging limit of AAV-mediated gene replacement therapy for neurological disorders
Author:
Affiliation:
1. Department of Neuroscience, Sheffield Institute for Translational Neuroscience (SITraN), University of Sheffield, Sheffield, UK
Funder
Maddi Foundation
British Neuropathological Society
European Research Council
MRC
IMI
Publisher
Informa UK Limited
Subject
Clinical Biochemistry,Drug Discovery,Pharmacology
Link
https://www.tandfonline.com/doi/pdf/10.1080/14712598.2022.2012148
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