Mutations in the glycosyltransferase domain of GLT8D1 are associated with familial amyotrophic lateral sclerosis

Cooper-Knock, J., Moll, T., Ramesh, T. et al. (26 more authors) (2019) Mutations in the glycosyltransferase domain of GLT8D1 are associated with familial amyotrophic lateral sclerosis. Cell Reports, 26 (9). 2298-2306.e5. ISSN 2211-1247

Abstract

Metadata

Authors/Creators:
Copyright, Publisher and Additional Information: © 2019 The Author(s). This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
Keywords: Amyotrophic lateral sclerosis; genetics; GLT8D1; glycosyltransferase; cell model; zebrafish
Dates:
  • Published (online): 26 February 2019
  • Published: 26 February 2019
  • Accepted: 30 January 2019
Institution: The University of Sheffield
Academic Units: The University of Sheffield > Sheffield Teaching Hospitals
Funding Information:
FunderGrant number
MOTOR NEURONE DISEASE ASSOCIATIONRamesh/Apr17/854-791
Depositing User: Symplectic Sheffield
Date Deposited: 28 Feb 2019 10:10
Last Modified: 13 Jan 2020 11:55
Published Version: https://doi.org/10.1016/j.celrep.2019.02.006
Status: Published
Publisher: Elsevier
Refereed: Yes
Identification Number: https://doi.org/10.1016/j.celrep.2019.02.006

Download

Share / Export

Statistics