FULL-LENGTH ORIGINAL RESEARCH
Electroclinical presentation and genotype–phenotype relationships in patients with Unverricht-Lundborg disease carrying compound heterozygous CSTB point and indel mutations
Article first published 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 published online: 3 DEC 2012
- Article first published online: 12 OCT 2012
- Accepted August 21, 2012; Early View publication October 12, 2012
Vol. 54, Issue 7, 1333, Article first published online: 1 JUL 2013
Figure S1. Polygraphic recordings.
|epi3718_sm_FigureS1.tif||390K||Supporting info item|
Please note: Wiley Blackwell is not responsible for the content or functionality of any supporting information supplied by the authors. Any queries (other than missing content) should be directed to the corresponding author for the article.