Please use this identifier to cite or link to this item:
https://hdl.handle.net/2440/106827
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Type: | Journal article |
Title: | Do mutations in SCN1B cause Dravet syndrome? |
Author: | Kim, Y. Dibbens, L. Marini, C. Suls, A. Chemaly, N. Mei, D. McMahon, J. Iona, X. Berkovic, S. De Jonghe, P. Guerrini, R. Nabbout, R. Scheffer, I. |
Citation: | Epilepsy Research, 2013; 103(1):97-100 |
Publisher: | Elsevier BV |
Issue Date: | 2013 |
ISSN: | 0920-1211 1872-6844 |
Statement of Responsibility: | Young Ok Kim, Leanne Dibbens, Carla Marini, Arvid Suls, Nicole Chemaly, Davide Mei, Jacinta M. McMahon, Xenia Iona, Samuel F. Berkovic, Peter De Jonghe, Renzo Guerrini, Rima Nabbout, Ingrid E. Scheffer |
Abstract: | Abstract not available |
Keywords: | SCN1B; Dravet syndrome; epileptic encephalopathy |
Description: | Available online 20 November 2012 |
Rights: | © 2012 Elsevier B.V. All rights reserved. |
DOI: | 10.1016/j.eplepsyres.2012.10.009 |
Appears in Collections: | Aurora harvest 3 Molecular and Biomedical Science publications |
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