Article info
PDFGenome-wide studies
Original article
Novel mutations consolidate KCTD7 as a progressive myoclonus epilepsy gene
- Correspondence to Professor Anna-Elina Lehesjoki, Folkhälsan Institute of Genetics, Biomedicum Helsinki, PO Box 63 (Haartmaninkatu 8), University of Helsinki, FIN-00014 Helsinki, Finland; anna-elina.lehesjoki{at}helsinki.fi
Citation
Novel mutations consolidate KCTD7 as a progressive myoclonus epilepsy gene
Publication history
- Received March 1, 2012
- Revised April 16, 2012
- Accepted April 18, 2012
- First published June 12, 2012.
Online issue publication
April 27, 2016
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
© 2012, 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.