Article info
PDFDevelopmental defects
Original article
Deletions and de novo mutations of SOX11 are associated with a neurodevelopmental disorder with features of Coffin–Siris syndrome
- 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
Citation
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
April 27, 2016
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Supplementary Data
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- Data supplement 1 - Online supplement
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