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
Published version: http://dx.doi.org/10.1016/j.eplepsyres.2012.10.009
Appears in Collections:Aurora harvest 3
Molecular and Biomedical Science publications

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