Extended spectrum of idiopathic generalized epilepsies associated with CACNA1H functional variants

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dc.contributor.authorHeron, Sarah E.
dc.contributor.authorKhosravani, Houman
dc.contributor.authorVarela, Diego L.
dc.contributor.authorBladen, Chris
dc.contributor.authorWilliams, Tristiana C.
dc.contributor.authorNewman, Michelle R.
dc.contributor.authorScheffer, Ingrid
dc.contributor.authorBerkovic, Samuel F.
dc.contributor.authorMulley, John C.
dc.contributor.authorZamponi, Gerald W.
dc.date.accessioned2018-06-07T17:21:24Z
dc.date.available2018-06-07T17:21:24Z
dc.date.issued2007-08-14
dc.description.abstractThe relationship between genetic variation in the T-type calcium channel gene CACNA1H and childhood absence epilepsy is well established. The purpose of this study was to investigate the range of epilepsy syndromes for which CACNA1H variants may contribute to the genetic susceptibility architecture and determine the electrophysiological effects of these variants in relation to proposed mechanisms underlying seizures.en_US
dc.identifier.citationHeron, S. E., Khosravani, H., Varela, D., Bladen, C., Williams, T. C., Newman, M. R., … Zamponi, G. W. (2007). Extended spectrum of idiopathic generalized epilepsies associated with CACNA1H functional variants. Annals of Neurology, 62(6), 560–568. https://doi.org/10.1002/ana.21169en_US
dc.identifier.doihttp://dx.doi.org/10.1002/ana.21169en_US
dc.identifier.issn0364-5134
dc.identifier.urihttp://hdl.handle.net/1880/106734
dc.language.isoenen_US
dc.publisherWiley-Liss, Inc.en_US
dc.publisher.departmentPhysiology & Pharmacologyen_US
dc.publisher.facultyCumming School of Medicineen_US
dc.publisher.institutionUniversity of Calgaryen_US
dc.publisher.policyhttp://olabout.wiley.com/WileyCDA/Section/id-826716.htmlen_US
dc.rights.urihttps://creativecommons.org/licenses/by/4.0en_US
dc.titleExtended spectrum of idiopathic generalized epilepsies associated with CACNA1H functional variantsen_US
dc.typejournal articleen_US
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