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dc.contributor.authorWang, Dan
dc.contributor.authorZhang, Feng
dc.contributor.authorGao, Guangping
dc.date.accessioned2022-05-16T19:31:26Z
dc.date.available2021-12-08T18:08:11Z
dc.date.available2022-05-16T19:31:26Z
dc.date.issued2020-04
dc.identifier.issn0092-8674
dc.identifier.urihttps://hdl.handle.net/1721.1/138388.2
dc.description.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.en_US
dc.language.isoen
dc.publisherElsevier BVen_US
dc.relation.isversionofhttp://dx.doi.org/10.1016/j.cell.2020.03.023en_US
dc.rightsCreative Commons Attribution-NonCommercial-NoDerivs Licenseen_US
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/4.0/en_US
dc.sourcePMCen_US
dc.titleCRISPR-Based Therapeutic Genome Editing: Strategies and In Vivo Delivery by AAV Vectorsen_US
dc.typeArticleen_US
dc.identifier.citationWang, D, Zhang, F and Gao, G. 2020. "CRISPR-Based Therapeutic Genome Editing: Strategies and In Vivo Delivery by AAV Vectors." Cell, 181 (1).en_US
dc.contributor.departmentMassachusetts Institute of Technology. Department of Brain and Cognitive Sciences
dc.contributor.departmentMassachusetts Institute of Technology. Department of Biological Engineering
dc.contributor.departmentMcGovern Institute for Brain Research at MIT
dc.contributor.departmentHoward Hughes Medical Institute
dc.relation.journalCellen_US
dc.eprint.versionAuthor's final manuscripten_US
dc.type.urihttp://purl.org/eprint/type/JournalArticleen_US
eprint.statushttp://purl.org/eprint/status/PeerRevieweden_US
dc.date.updated2021-12-08T18:05:55Z
dspace.orderedauthorsWang, D; Zhang, F; Gao, Gen_US
dspace.date.submission2021-12-08T18:05:56Z
mit.journal.volume181en_US
mit.journal.issue1en_US
mit.licensePUBLISHER_CC
mit.metadata.statusAuthority Work Neededen_US


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