PRRT2 mutations and paroxysmal disorders
Version of Record online: 9 FEB 2013
© 2013 The Author(s) European Journal of Neurology © 2013 EFNS
European Journal of Neurology
Volume 20, Issue 6, pages 872–878, June 2013
How to Cite
Méneret, A., Gaudebout, C., Riant, F., Vidailhet, M., Depienne, C. and Roze, E. (2013), PRRT2 mutations and paroxysmal disorders. European Journal of Neurology, 20: 872–878. doi: 10.1111/ene.12104
- Issue online: 12 MAY 2013
- Version of Record online: 9 FEB 2013
- Manuscript Accepted: 17 DEC 2012
- Manuscript Received: 27 AUG 2012
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