MYT1L mutations cause intellectual disability and variable obesity by dysregulating gene expression and development of the neuroendocrine hypothalamus

Blanchet, P., Bebin, M., Bruet, S, et al. (16 more authors) (2017) MYT1L mutations cause intellectual disability and variable obesity by dysregulating gene expression and development of the neuroendocrine hypothalamus. PLoS Genetics, 13 (8). e1006957. ISSN 1553-7390

Abstract

Metadata

Authors/Creators:
  • Blanchet, P.
  • Bebin, M.
  • Bruet, S,
  • Cooper, G.M.
  • Thompson, M.L.
  • Duban-Bedu, B.
  • Gerard, B.
  • Piton, A.
  • Suckno, S.
  • Deshpande, C.
  • Clowes, V.
  • Vogt, J.
  • Turnpenny, P.
  • Williamson, M.P.
  • Alembik, Y.
  • Consortium, C.S.E.R.S.
  • Consortium, D.D.D.
  • Glasgow, E.
  • McNeill, A.
Copyright, Publisher and Additional Information: © 2017 Blanchet et al. This is an open access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
Dates:
  • Accepted: 4 August 2017
  • Published (online): 31 August 2017
  • Published: 31 August 2017
Institution: The University of Sheffield
Academic Units: The University of Sheffield > Faculty of Medicine, Dentistry and Health (Sheffield) > Department of Neuroscience (Sheffield)
Funding Information:
FunderGrant number
NEWLIFE FOUNDATION FOR DISABLED CHILDRENSG/15-16/07
Depositing User: Symplectic Sheffield
Date Deposited: 25 Aug 2017 11:33
Last Modified: 14 Jul 2020 16:54
Published Version: https://doi.org/10.1371/journal.pgen.1006957
Status: Published
Publisher: Public Library of Science (PLoS)
Refereed: Yes
Identification Number: https://doi.org/10.1371/journal.pgen.1006957
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