SLC35A2-related congenital disorder of glycosylation: Defining the phenotype

Yates, T.M., Suri, M., Desurkar, A. et al. (8 more authors) (2018) SLC35A2-related congenital disorder of glycosylation: Defining the phenotype. European Journal of Paediatric Neurology. ISSN 1090-3798

Abstract

Metadata

Authors/Creators:
  • Yates, T.M.
  • Suri, M.
  • Desurkar, A.
  • Lesca, G.
  • Wallgren-Pettersson, C.
  • Hammer, T.B.
  • Raghavan, A.
  • Poulat, A.-L.
  • Møller, R.S.
  • Thuresson, A.-C.
  • Balasubramanian, M. https://orcid.org/0000-0003-1488-3695
Copyright, Publisher and Additional Information: © 2018 Elsevier. This is an author produced version of a paper subsequently published in European Journal of Paediatric Neurology. Uploaded in accordance with the publisher's self-archiving policy. Article available under the terms of the CC-BY-NC-ND licence (https://creativecommons.org/licenses/by-nc-nd/4.0/).
Keywords: Congenital disorders of glycosylation; Developmental and epileptic encephalopathy; Intellectual disability; SLC35A2
Dates:
  • Accepted: 19 August 2018
  • Published (online): 27 August 2018
Institution: The University of Sheffield
Depositing User: Symplectic Sheffield
Date Deposited: 17 Sep 2018 11:59
Last Modified: 27 Aug 2019 00:42
Published Version: https://doi.org/10.1016/j.ejpn.2018.08.002
Status: Published online
Publisher: Elsevier
Refereed: Yes
Identification Number: https://doi.org/10.1016/j.ejpn.2018.08.002
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