Do mutations in SCN1B cause Dravet syndrome?

Simple item page
dc.contributor.authorKim, Y.
dc.contributor.authorDibbens, L.
dc.contributor.authorMarini, C.
dc.contributor.authorSuls, A.
dc.contributor.authorChemaly, N.
dc.contributor.authorMei, D.
dc.contributor.authorMcMahon, J.
dc.contributor.authorIona, X.
dc.contributor.authorBerkovic, S.
dc.contributor.authorDe Jonghe, P.
dc.contributor.authorGuerrini, R.
dc.contributor.authorNabbout, R.
dc.contributor.authorScheffer, I.
dc.date.issued2013
dc.descriptionAvailable online 20 November 2012
dc.description.abstractAbstract not available
dc.description.statementofresponsibilityYoung 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
dc.identifier.citationEpilepsy Research, 2013; 103(1):97-100
dc.identifier.doi10.1016/j.eplepsyres.2012.10.009
dc.identifier.issn0920-1211
dc.identifier.issn1872-6844
dc.identifier.urihttp://hdl.handle.net/2440/106827
dc.language.isoen
dc.publisherElsevier BV
dc.rights© 2012 Elsevier B.V. All rights reserved.
dc.source.urihttps://doi.org/10.1016/j.eplepsyres.2012.10.009
dc.subjectSCN1B; Dravet syndrome; epileptic encephalopathy
dc.titleDo mutations in SCN1B cause Dravet syndrome?
dc.typeJournal article
pubs.publication-statusPublished

Files

Collections

Molecular and Biomedical Science publications