FULL-LENGTH ORIGINAL RESEARCH
Electroclinical presentation and genotype–phenotype relationships in patients with Unverricht-Lundborg disease carrying compound heterozygous CSTB point and indel mutations
Version of Record online: 12 OCT 2012
Wiley Periodicals, Inc. © 2012 International League Against Epilepsy
Volume 53, Issue 12, pages 2120–2127, December 2012
How to Cite
Canafoglia, L., Gennaro, E., Capovilla, G., Gobbi, G., Boni, A., Beccaria, F., Viri, M., Michelucci, R., Agazzi, P., Assereto, S., Coviello, D. A., Di Stefano, M., Rossi Sebastiano, D., Franceschetti, S. and Zara, F. (2012), Electroclinical presentation and genotype–phenotype relationships in patients with Unverricht-Lundborg disease carrying compound heterozygous CSTB point and indel mutations. Epilepsia, 53: 2120–2127. doi: 10.1111/j.1528-1167.2012.03718.x
- Issue online: 3 DEC 2012
- Version of Record online: 12 OCT 2012
- Accepted August 21, 2012; Early View publication October 12, 2012
Vol. 54, Issue 7, 1333, Version of Record online: 1 JUL 2013
Figure S1. Polygraphic recordings.
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