Exploring the association between SRPX2 variants and neurodevelopment: How causal is it?

Schirwani, S., McConnell, V., Willoughby, J. et al. (2 more authors) (2019) Exploring the association between SRPX2 variants and neurodevelopment: How causal is it? Gene, 685. pp. 50-54. ISSN 0378-1119

Abstract

Metadata

Authors/Creators:
Copyright, Publisher and Additional Information: © 2018 Elsevier.
Keywords: SRPX2; Rolandic epilepsy; Seizures; Speech and language impairment; Neurodevelopmental delay; FOXP2
Dates:
  • Accepted: 24 October 2018
  • Published (online): 25 October 2018
  • Published: 15 February 2019
Institution: The University of Sheffield
Academic Units: The University of Sheffield > Faculty of Medicine, Dentistry and Health (Sheffield) > Department of Human Metabolism (Sheffield)
Depositing User: Symplectic Sheffield
Date Deposited: 13 Feb 2019 11:56
Last Modified: 13 Feb 2019 11:56
Published Version: https://doi.org/10.1016/j.gene.2018.10.067
Status: Published
Publisher: Elsevier
Refereed: Yes
Identification Number: https://doi.org/10.1016/j.gene.2018.10.067
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