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CRISPR-Based Therapeutic Genome Editing: Strategies and In Vivo Delivery by AAV Vectors
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CRISPR-Based Therapeutic Genome Editing: Strategies and In Vivo Delivery by AAV Vectors
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Name
nihms-1576523.pdf
Description
Accepted version
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965.01 KB
Format
Adobe PDF
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2bc906abcd25b6ed36a643259d599422
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sword-2021-12-08T18:05:55.original.xml (130 B)
Original SWORD entry document
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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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Terms of Use
Creative Commons Attribution-NonCommercial-NoDerivs License
http://creativecommons.org/licenses/by-nc-nd/4.0/
Persistent DSpace Link
https://hdl.handle.net/1721.1/138388
DOI of Published Version
10.1016/j.cell.2020.03.023
