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Original article
De novo and rare inherited mutations implicate the transcriptional coregulator TCF20/SPBP in autism spectrum disorder

Authors

  1. 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
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Citation

Babbs C, Lloyd D, Pagnamenta AT, et al
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 
October 14, 2014

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