Epilepsy-causing STX1B mutations translate altered protein functions into distinct phenotypes in mouse neurons

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dc.contributor.author Schubert, Julian
dc.contributor.author Lerche, Holger
dc.date.accessioned 2021-06-22T06:56:37Z
dc.date.available 2021-06-22T06:56:37Z
dc.date.issued 2020
dc.identifier.issn 1460-2156
dc.identifier.uri http://hdl.handle.net/10900/116384
dc.language.iso en de_DE
dc.publisher Oxford Univ Press de_DE
dc.relation.uri http://dx.doi.org/10.1093/brain/awaa151 de_DE
dc.subject.ddc 570 de_DE
dc.subject.ddc 610 de_DE
dc.title Epilepsy-causing STX1B mutations translate altered protein functions into distinct phenotypes in mouse neurons de_DE
dc.type Artikel de_DE
utue.quellen.id 20210304112512_01805
utue.publikation.seiten 2119-2138 de_DE
utue.personen.roh Vardar, Gulcin
utue.personen.roh Gerth, Fabian
utue.personen.roh Schmitt, Xiao Jakob
utue.personen.roh Rautenstrauch, Pia
utue.personen.roh Trimbuch, Thorsten
utue.personen.roh Schubert, Julian
utue.personen.roh Lerche, Holger
utue.personen.roh Rosenmund, Christian
utue.personen.roh Freund, Christian
dcterms.isPartOf.ZSTitelID Brain de_DE
dcterms.isPartOf.ZS-Issue 7 de_DE
dcterms.isPartOf.ZS-Volume 143 de_DE
utue.fakultaet 04 Medizinische Fakultät de_DE


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