Gene Therapy for Familial ALS Using AAV9 Mediated Silencing of Mutant SOD1

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

Authors/Creators:
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:
  • Published: 18 July 2016
  • Published (online): 15 June 2016
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:
FunderGrant number
MEDICAL RESEARCH COUNCILMR/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: https://doi.org/10.1089/hum.2016.29027.abstracts
Related URLs:

Share / Export

Statistics