Conference item : Abstract
Genome editing of the liver for treatment of alpha-1 antitrypsin deficiency using homology-independent targeted integration (HITI)
- Publication status:
- Published
- Peer review status:
- Reviewed (other)
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Access Document
- Files:
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(Preview, Accepted manuscript, pdf, 100.8KB, Terms of use)
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- Publisher copy:
- 10.1016/j.ymthe.2019.04.004
Authors
- Publisher:
- Elsevier
- Host title:
- Molecular Therapy
- Journal:
- Molecular Therapy More from this journal
- Volume:
- 27
- Issue:
- 4-S1
- Pages:
- 464
- Publication date:
- 2019-04-12
- Acceptance date:
- 2019-03-20
- DOI:
- EISSN:
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1525-0024
- ISSN:
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1525-0016
- Language:
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English
- Keywords:
- Subtype:
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Abstract
- Pubs id:
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pubs:1015797
- UUID:
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uuid:d1ee871b-4a37-4546-a3da-b1108414fc3e
- Local pid:
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pubs:1015797
- Source identifiers:
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1015797
- Deposit date:
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2019-06-18
- ARK identifier:
Terms of use
- Copyright holder:
- van Haasteren et al.
- Copyright date:
- 2019
- Rights statement:
- © 2019 The Author(s).
- Notes:
- This item is the abstract for a paper presented at the 22nd American Society of Gene and Cell Therapy Annual Meeting (ASGCT 2019), Washington DC, USA, April-May 2019. This is the accepted manuscript version of the abstract available under a Creative Commons, Attribution, Non-Commercial, No-Derivatives licence. The final version is available online from Elsevier at: https://doi.org/10.1016/j.ymthe.2019.04.004
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