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dc.contributor.authorTürkdoğan, Dilşad
dc.contributor.authorUsluer, Sunay
dc.contributor.authorAkalın, Figen
dc.contributor.authorAğyüz, Umut
dc.contributor.authorAslan, Elif Sibel
dc.date.accessioned30.04.201910:49:13
dc.date.accessioned2019-05-30T20:40:11Z
dc.date.available30.04.201910:49:13
dc.date.available2019-05-30T20:40:11Z
dc.date.issued2017
dc.identifier.issn1059-1311
dc.identifier.issn1532-2688
dc.identifier.urihttps://doi.org/10.1016/j.seizure.2017.06.019
dc.identifier.urihttps://hdl.handle.net/20.500.12445/757
dc.descriptionThe authors disclosed receipt of the following financial support for the research of this article: Whole-exome sequencing in three cases was included in the project, titled 'Investigation of genetic etiology in patients with Epileptic Encephalopaties using Whole-Exome Sequencing'. D. Turkdogan executed this project granted by the Scientific and Technological Research Council of Turkey (Project No. 214S624).en_US
dc.description.sponsorshipScientific and Technological Research Council of Turkey [214S624]en_US
dc.language.isoengen_US
dc.publisherElsevier B.V.en_US
dc.relation.isversionof10.1016/j.seizure.2017.06.019en_US
dc.rightsinfo:eu-repo/semantics/closedAccessen_US
dc.subjectSudden Death in Epilepsyen_US
dc.subjectGNB5 Geneen_US
dc.subjectGenetic Diagnosisen_US
dc.subjectEarly Onset Epileptic Encephalopathyen_US
dc.subjectCardiac Arrhythmiaen_US
dc.titleFamilial early infantile epileptic encephalopathy and cardiac conduction disorder: A rare cause of SUDEP in infancyen_US
dc.typearticleen_US
dc.relation.journalSeizure-European Journal of Epilepsyen_US
dc.contributor.departmentBiruni Üniversitesien_US
dc.identifier.volume50en_US
dc.identifier.startpage171en_US
dc.identifier.endpage172en_US
dc.relation.tubitakScientific and Technological Research Council of Turkey [214S624]en_US
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US


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