Iannitti, T., Scarrot, J.M., Coldicott, I.R.P. et al. (4 more authors) (2016) Gene Therapy for Familial ALS Using AAV9 Mediated Silencing of Mutant SOD1. In: Human Gene Therapy. British Society for Gene and Cell Therapy Annual Conference, 15th April 2016, University College London Institute of Child Health. Mary Ann Liebert Inc , A12-A12.
Metadata
Item Type: | Proceedings Paper |
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Authors/Creators: |
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Copyright, Publisher and Additional Information: | © 2016 Mary Ann Liebert Inc. This is an author produced version of a paper subsequently published in Human Gene Therapy. Uploaded in accordance with the publisher's self-archiving policy. |
Dates: |
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Institution: | The University of Sheffield |
Academic Units: | The University of Sheffield > Faculty of Medicine, Dentistry and Health (Sheffield) > Department of Neuroscience (Sheffield) The University of Sheffield > Sheffield Teaching Hospitals |
Funding Information: | Funder Grant number MEDICAL RESEARCH COUNCIL MR/K000039/1 |
Depositing User: | Symplectic Sheffield |
Date Deposited: | 02 Nov 2016 10:45 |
Last Modified: | 18 Jul 2017 10:23 |
Published Version: | http://dx.doi.org/10.1089/hum.2016.29027.abstracts |
Status: | Published |
Publisher: | Mary Ann Liebert Inc |
Refereed: | Yes |
Identification Number: | 10.1089/hum.2016.29027.abstracts |
Related URLs: | |
Open Archives Initiative ID (OAI ID): | oai:eprints.whiterose.ac.uk:106640 |