ZMYND11 variants are a novel cause of centrotemporal and generalised epilepsies with neurodevelopmental disorder

Oates, S., Absoud, M., Goyal, S. et al. (32 more authors) (2021) ZMYND11 variants are a novel cause of centrotemporal and generalised epilepsies with neurodevelopmental disorder. Clinical Genetics. ISSN 0009-9163

Abstract

Metadata

Authors/Creators:
  • Oates, S.
  • Absoud, M.
  • Goyal, S.
  • Bayley, S.
  • Baulcomb, J.
  • Sims, A.
  • Riddett, A.
  • Allis, K.
  • Brasch Andersen, C.
  • Balasubramanian, M. ORCID logo https://orcid.org/0000-0003-1488-3695
  • Bai, R.
  • Callewaert, B.
  • Hüffmeier, U.
  • LeDuc, D.
  • Radtke, M.
  • Korff, C.
  • Kennedy, J.
  • Low, K.
  • Møller, R.
  • Nielsen, J.E.K.
  • Popp, B.
  • Quteineh, L.
  • Rønde, G.
  • Schönewolf‐Greulich, B.
  • Shillington, A.
  • Taylor, M.R.G.
  • Todd, E.
  • Toerring, P.M.
  • Tümer, Z.
  • Vasileiou, G.
  • Yates, T.M.
  • Zweier, C.
  • Rosch, R.
  • Basson, M.A.
  • Pal, D.K.
Copyright, Publisher and Additional Information: © 2021 John Wiley & Sons A/S. Published by John Wiley & Sons Ltd. This is an author-produced version of a paper subsequently published in Clinical Genetics. Uploaded in accordance with the publisher's self-archiving policy.
Keywords: epigenetic; seizure; EEG; antiepileptic drug; comorbidity; autism; histone H3.3; bromodomain
Dates:
  • Accepted: 30 June 2021
  • Published (online): 16 July 2021
Institution: The University of Sheffield
Academic Units: The University of Sheffield > Faculty of Medicine, Dentistry and Health (Sheffield) > Department of Human Metabolism (Sheffield)
The University of Sheffield > Faculty of Medicine, Dentistry and Health (Sheffield) > Department of Oncology (Sheffield)
Depositing User: Symplectic Sheffield
Date Deposited: 15 Jul 2021 17:07
Last Modified: 03 Aug 2021 16:22
Status: Published online
Publisher: Wiley
Refereed: Yes
Identification Number: https://doi.org/10.1111/cge.14023
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