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CRISPR-Based Therapeutic Genome Editing: Strategies and In Vivo Delivery by AAV Vectors

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sword-2021-12-08T18:05:55.original.xml (130 B)
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Author(s)
Wang, D
•
Zhang, F
•
Gao, G
Date Issued
April 2, 2020
Journal
Cell
Publisher
Elsevier BV
Citation
Wang, D, Zhang, F and Gao, G. 2020. "CRISPR-Based Therapeutic Genome Editing: Strategies and In Vivo Delivery by AAV Vectors." Cell, 181 (1).
Version
Author's final manuscript
Abstract
© 2020 Elsevier Inc. Wang, Zhang, and Gao discuss the progress, concerns, and challenges currently facing CRISPR-based therapeutics, a field that has inspired renewed but cautious interest in human genome editing.
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Creative Commons Attribution-NonCommercial-NoDerivs License
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DOI of Published Version
10.1016/j.cell.2020.03.023
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