ZMYND11‐related syndromic intellectual disability: 16 patients delineating and expanding the phenotypic spectrum

Yates, T.M., Drucker, M., Barnicoat, A. et al. (19 more authors) (2020) ZMYND11‐related syndromic intellectual disability: 16 patients delineating and expanding the phenotypic spectrum. Human Mutation. ISSN 1059-7794

Abstract

Metadata

Authors/Creators:
  • Yates, T.M.
  • Drucker, M.
  • Barnicoat, A.
  • Low, K.
  • Gerkes, E.H.
  • Fry, A.E.
  • Parker, M.J.
  • Driscoll, M.O.
  • Charles, P.
  • Cox, H.
  • Marey, I.
  • Keren, B.
  • Rinne, T.
  • McEntagart, M.
  • Ramachandran, V.
  • Drury, S.
  • Vansenne, F.
  • Sival, D.A.
  • Herkert, J.C.
  • Callewaert, B.
  • Tan, W.
  • Balasubramanian, M. https://orcid.org/0000-0003-1488-3695
Copyright, Publisher and Additional Information: © 2020 Wiley Periodicals, Inc. This is an author-produced version of a paper subsequently published in Human Mutation. Uploaded in accordance with the publisher's self-archiving policy.
Keywords: Behavioral Symptoms; Gene Expression Regulation; Intellectual Disability; Seizures; Zinc Fingers
Dates:
  • Published (online): 25 February 2020
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: 04 Mar 2020 14:40
Last Modified: 04 Mar 2020 14:40
Status: Published online
Publisher: Wiley
Refereed: Yes
Identification Number: https://doi.org/10.1002/humu.24001
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