Article info
PDFCognitive and behavioural genetics
Original article
De novo and rare inherited mutations implicate the transcriptional coregulator TCF20/SPBP in autism spectrum disorder
- Correspondence to Prof Andrew O M Wilkie, Weatherall Institute of Molecular Medicine, University of Oxford, John Radcliffe Hospital, Oxford, UK, OX3 9DS, UK; andrew.wilkie{at}imm.ox.ac.uk Dr Jeremy R Parr, Institute of Neuroscience, Newcastle University, Newcastle Upon Tyne, NE1 7RU, UK; jeremy.parr@newcastle.ac.uk
Citation
De novo and rare inherited mutations implicate the transcriptional coregulator TCF20/SPBP in autism spectrum disorder
Publication history
- Received June 10, 2014
- Revised August 13, 2014
- Accepted August 13, 2014
- First published September 16, 2014.
Online issue publication
November 15, 2016
Article Versions
- Previous version (27 April 2016).
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- Data supplement 1 - Online supplement
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Published by the BMJ Publishing Group Limited. For permission to use (where not already granted under a licence) please go to http://group.bmj.com/group/rights-licensing/permissions This is an Open Access article distributed in accordance with the terms of the Creative Commons Attribution (CC BY 4.0) license, which permits others to distribute, remix, adapt and build upon this work, for commercial use, provided the original work is properly cited. See: http://creativecommons.org/licenses/by/4.0/