MBdP, SG, AS and CC contributed equally to this study.
Letter to the Editor
A novel compound heterozygous mutation of C20orf54 gene associated with Brown–Vialetto–Van Laere syndrome in an Italian family
Article first published online: 10 JUN 2013
© 2013 The Author(s) European Journal of Neurology © 2013 EFNS
European Journal of Neurology
Volume 20, Issue 7, pages e94–e95, July 2013
How to Cite
Bandettini di Poggio, M., Gagliardi, S., Pardini, M., Marchioni, E., Monti Bragadin, M., Reni, L., Doria-Lamba, L., Roccatagliata, L., Ceroni, M., Schenone, A. and Cereda, C. (2013), A novel compound heterozygous mutation of C20orf54 gene associated with Brown–Vialetto–Van Laere syndrome in an Italian family. European Journal of Neurology, 20: e94–e95. doi: 10.1111/ene.12163
- Issue published online: 10 JUN 2013
- Article first published online: 10 JUN 2013
- Manuscript Accepted: 28 FEB 2013
- Manuscript Received: 27 SEP 2012
- Italian Ministry of Health
- National Institute of Neurology Foundation
- the Italian Telethon. Grant Numbers: GGP02169, GUP04002
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