Further delineation of phenotypic spectrum of SCN2A-related disorder

Richardson, R., Baralle, D., Bennett, C. et al. (19 more authors) (2022) Further delineation of phenotypic spectrum of SCN2A-related disorder. American Journal of Medical Genetics Part A, 188 (3). pp. 867-877. ISSN 1552-4825

Abstract

Metadata

Authors/Creators:
  • Richardson, R.
  • Baralle, D.
  • Bennett, C.
  • Briggs, T.
  • Bijlsma, E.K.
  • Clayton‐Smith, J.
  • Constantinou, P.
  • Foulds, N.
  • Jarvis, J.
  • Jewell, R.
  • Johnson, D.S.
  • McEntagart, M.
  • Parker, M.J.
  • Radley, J.A.
  • Robertson, L.
  • Ruivenkamp, C.
  • Rutten, J.W.
  • Tellez, J.
  • Turnpenny, P.D.
  • Wilson, V.
  • Wright, M.
  • Balasubramanian, M. ORCID logo https://orcid.org/0000-0003-1488-3695
Copyright, Publisher and Additional Information: © 2021 Wiley Periodicals LLC. This is an author-produced version of a paper subsequently published in American Journal of Medical Genetics Part A. Uploaded in accordance with the publisher's self-archiving policy.
Keywords: autism spectrum disorder; developmental delay; episodic ataxia; intellectual disability; SCN2A
Dates:
  • Accepted: 20 November 2021
  • Published (online): 11 December 2021
  • Published: 11 February 2022
Institution: The University of Sheffield
Academic Units: The University of Sheffield > Faculty of Medicine, Dentistry and Health (Sheffield)
Depositing User: Symplectic Sheffield
Date Deposited: 26 Apr 2022 12:07
Last Modified: 11 Dec 2022 01:13
Status: Published
Publisher: Wiley
Refereed: Yes
Identification Number: https://doi.org/10.1002/ajmg.a.62595

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