Members of the EMINet Consortium are in Appendix 1.
Full-Length Original Research
Rare exonic deletions of the RBFOX1 gene increase risk of idiopathic generalized epilepsy
Version of Record online: 25 JAN 2013
Wiley Periodicals, Inc. © 2013 International League Against Epilepsy
Volume 54, Issue 2, pages 265–271, February 2013
How to Cite
Lal, D., Trucks, H., Møller, R. S., Hjalgrim, H., Koeleman, B. P. C., de Kovel, C. G. F., Visscher, F., Weber, Y. G., Lerche, H., Becker, F., Schankin, C. J., Neubauer, B. A., Surges, R., Kunz, W. S., Zimprich, F., Franke, A., Illig, T., Ried, J. S., Leu, C., Nürnberg, P., Sander, T., EMINet Consortium and EPICURE Consortium (2013), Rare exonic deletions of the RBFOX1 gene increase risk of idiopathic generalized epilepsy. Epilepsia, 54: 265–271. doi: 10.1111/epi.12084
- Issue online: 5 FEB 2013
- Version of Record online: 25 JAN 2013
- Manuscript Accepted: 21 NOV 2012
- European Community. Grant Number: LSHM-CT-2006-037315
- German Research Foundation . Grant Numbers: NE416/5-1, Le1030/11-1, SA434/5-1
- German Federal Ministry of Education and Research
- National Genome Research Network. Grant Numbers: 01GS08120, 01GS08123, TUR 09/I10
- The Netherlands National Epilepsy Fund. Grant Number: 04-08
- The Netherlands Organization for Scientific Research. Grant Number: 917.66.315
- PopGen biobank
- Munich Center of Health Sciences
Figure S1. Overview of all deletions affecting the RBFOX1 gene including locations of the TaqMan qPCR assays.
Figure S2. Raw signal intensity data of all samples carrying exon-disrupting deletions affecting the RBFOX1 gene.
Figure S3. UCSC Genome Browser RBFOX1 regulatory annotation tracks.
Table S1. Epilepsy phenotype of individuals examined by qPCR and overview of all RBFOX1 deletions validated by TaqMan qPCR assays.
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