Article info
PDFNovel disease loci
Short report
De novo variants in SUPT16H cause neurodevelopmental disorders associated with corpus callosum abnormalities
- Correspondence to Dr Elliott H. Sherr, Neurology, UCSF, San Francisco, CA 94158, USA; Elliott.Sherr{at}ucsf.edu
Citation
De novo variants in SUPT16H cause neurodevelopmental disorders associated with corpus callosum abnormalities
Publication history
- Received April 1, 2019
- Revised October 29, 2019
- Accepted November 17, 2019
- First published January 10, 2020.
Online issue publication
June 23, 2020
Article Versions
- Previous version (23 June 2020).
- You are viewing the most recent version of this article.
Request permissions
If you wish to reuse any or all of this article please use the link below which will take you to the Copyright Clearance Center’s RightsLink service. You will be able to get a quick price and instant permission to reuse the content in many different ways.
Copyright information
© Author(s) (or their employer(s)) 2020. No commercial re-use. See rights and permissions. Published by BMJ.