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dc.contributor.CRUESPUniversidade Estadual de Campinaspt_BR
dc.typeArtigo de periódicopt_BR
dc.titleTHE SCN2A gene is not a likely candidate for familial mesial temporal lobe epilepsypt_BR
dc.contributor.authorMaurer-Morelli, CVpt_BR
dc.contributor.authorSecolin, Rpt_BR
dc.contributor.authorMarchesini, RBpt_BR
dc.contributor.authorSantos, NFpt_BR
dc.contributor.authorKobayashi, Ept_BR
dc.contributor.authorCendes, Fpt_BR
dc.contributor.authorLopes-Cendes, Ipt_BR
unicamp.author.emailicendes@unicamp.brpt_BR
unicamp.authorUniv Estadual Campinas, Dept Med Genet, BR-13084971 Campinas, SP, Brazil Univ Estadual Campinas, Dept Neurol, Campinas, SP, Brazilpt_BR
dc.subjectcandidate locuspt_BR
dc.subjectgeneticspt_BR
dc.subjectmicrosatellitespt_BR
dc.subjectlinkage studypt_BR
dc.subjectvoltage-gated sodium channelpt_BR
dc.subjecthippocampal sclerosispt_BR
dc.subject.wosResonance-imaging Evidencept_BR
dc.subject.wosHippocampal Sclerosispt_BR
dc.subject.wosFebrile Convulsionspt_BR
dc.subject.wosSurgical-treatmentpt_BR
dc.subject.wosAbnormalitiespt_BR
dc.subject.wosAtrophypt_BR
dc.description.abstractA transgenic mouse model carrying a mutation in the Scn2a gene showed chronic focal seizures associated with extensive cell loss and gliosis in the hippocampus, a similar phenotype found in familial mesial temporal lobe epilepsy (FMTLE). Our objective was to test whether the human homolog of the Scn2a gene is responsible for hippocampal abnormalities in FMTLE by linkage analysis. We conclusively ruled out the SCN2A gene as candidate in FMTLE. (c) 2006 Elsevier B.V. All rights reserved.pt
dc.relation.ispartofEpilepsy Researchpt_BR
dc.relation.ispartofabbreviationEpilepsy Res.pt_BR
dc.publisher.cityAmsterdampt_BR
dc.publisher.countryHolandapt_BR
dc.publisherElsevier Science Bvpt_BR
dc.date.issued2006pt_BR
dc.date.monthofcirculationOCTpt_BR
dc.identifier.citationEpilepsy Research. Elsevier Science Bv, v. 71, n. 41700, n. 233, n. 236, 2006.pt_BR
dc.language.isoenpt_BR
dc.description.volume71pt_BR
dc.description.issuenumber41700pt_BR
dc.description.firstpage233pt_BR
dc.description.lastpage236pt_BR
dc.rightsfechadopt_BR
dc.rights.licensehttp://www.elsevier.com/about/open-access/open-access-policies/article-posting-policypt_BR
dc.sourceWeb of Sciencept_BR
dc.identifier.issn0920-1211pt_BR
dc.identifier.wosidWOS:000241310300017pt_BR
dc.identifier.doi10.1016/j.eplepsyres.2006.06.016pt_BR
dc.date.available2014-11-16T06:59:06Z
dc.date.available2015-11-26T16:20:41Z-
dc.date.accessioned2014-11-16T06:59:06Z
dc.date.accessioned2015-11-26T16:20:41Z-
dc.description.provenanceMade available in DSpace on 2014-11-16T06:59:06Z (GMT). No. of bitstreams: 1 WOS000241310300017.pdf: 115936 bytes, checksum: 2553cedef56400740115c41155026378 (MD5) Previous issue date: 2006en
dc.description.provenanceMade available in DSpace on 2015-11-26T16:20:41Z (GMT). No. of bitstreams: 2 WOS000241310300017.pdf: 115936 bytes, checksum: 2553cedef56400740115c41155026378 (MD5) WOS000241310300017.pdf.txt: 13957 bytes, checksum: b5a17da4f7ba8c1f1ad9e0d93f88e92d (MD5) Previous issue date: 2006en
dc.identifier.urihttp://www.repositorio.unicamp.br/jspui/handle/REPOSIP/72430pt_BR
dc.identifier.urihttp://www.repositorio.unicamp.br/handle/REPOSIP/72430
dc.identifier.urihttp://repositorio.unicamp.br/jspui/handle/REPOSIP/72430-
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