Full-Length Original Research
A novel pedigree with familial cortical myoclonic tremor and epilepsy (FCMTE): Clinical characterization, refinement of the FCMTE2 locus, and confirmation of a founder haplotype
Version of Record online: 11 MAY 2013
Wiley Periodicals, Inc. © 2013 International League Against Epilepsy
Volume 54, Issue 7, pages 1298–1306, July 2013
How to Cite
Licchetta, L., Pippucci, T., Bisulli, F., Cantalupo, G., Magini, P., Alvisi, L., Baldassari, S., Martinelli, P., Naldi, I., Vanni, N., Liguori, R., Seri, M. and Tinuper, P. (2013), A novel pedigree with familial cortical myoclonic tremor and epilepsy (FCMTE): Clinical characterization, refinement of the FCMTE2 locus, and confirmation of a founder haplotype. Epilepsia, 54: 1298–1306. doi: 10.1111/epi.12216
- Issue online: 1 JUL 2013
- Version of Record online: 11 MAY 2013
- Manuscript Accepted: 2 APR 2013
- Italian Ministry of Health, Young Investigators Award. Grant Number: GR-2009-1574072
Vol. 54, Issue 9, 1709, Version of Record online: 6 SEP 2013
Table S1. LOD score values for the 22 markers distributed across the FCMTE1, FCMTE2 and FCMTE3 locus.
Table S2. Linkage and haplotype analysis in the extended pedigree.
Data S1. Neurophysiological testing—methods.
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.