These authors contributed equally to this work.
A homozygous mutation of voltage-gated sodium channel βI gene SCN1B in a patient with Dravet syndrome
Article first published online: 13 NOV 2012
Wiley Periodicals, Inc. © 2012 International League Against Epilepsy
Volume 53, Issue 12, pages e200–e203, December 2012
How to Cite
Ogiwara, I., Nakayama, T., Yamagata, T., Ohtani, H., Mazaki, E., Tsuchiya, S., Inoue, Y. and Yamakawa, K. (2012), A homozygous mutation of voltage-gated sodium channel βI gene SCN1B in a patient with Dravet syndrome. Epilepsia, 53: e200–e203. doi: 10.1111/epi.12040
- Issue published online: 3 DEC 2012
- Article first published online: 13 NOV 2012
- Accepted September 27, 2012; Early View publication November 13, 2012.
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