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Original article
Deletions and de novo mutations of SOX11 are associated with a neurodevelopmental disorder with features of Coffin–Siris syndrome

Authors

  1. Correspondence to Dr Alisdair McNeill, Sheffield Institute for Translational Neuroscience, 385a Glossop Road, Sheffield, South Yorkshire S11 9LE, UK; a.mcneill{at}sheffield.ac.uk
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Citation

Hempel A, Pagnamenta AT, Blyth M, et al
Deletions and de novo mutations of SOX11 are associated with a neurodevelopmental disorder with features of Coffin–Siris syndrome

Publication history

  • Received July 16, 2015
  • Revised September 9, 2015
  • Accepted September 11, 2015
  • First published November 5, 2015.
Online issue publication 
February 24, 2016

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