Article info
Epilepsy
Short report
PRRT2 mutations: exploring the phenotypical boundaries
- Correspondence to Dr Arvid Suls, Neurogenetics Group, VIB-Department of Molecular Genetics, University of Antwerp, Campus CDE, Parking P4, Building V1.33, Universiteitsplein 1, Antwerp 2610, Belgium; arvid.suls{at}molgen.vib-ua.be
Citation
PRRT2 mutations: exploring the phenotypical boundaries
Publication history
- Received February 5, 2013
- Revised June 21, 2013
- Accepted September 10, 2013
- First published October 7, 2013.
Online issue publication
April 13, 2016
Article Versions
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