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.
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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. | ||||
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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 |
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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: | https://doi.org/10.1089/hum.2016.29027.abstracts | ||||
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