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

Vardar, Gulcin; Gerth, Fabian; Schmitt, Xiao Jakob; Rautenstrauch, Pia; Trimbuch, Thorsten; Schubert, Julian; Lerche, Holger; Rosenmund, Christian; Freund, Christian

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	Article	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