Homozygous mutation in TXNRD1 is associated with genetic generalized epilepsy

Kudin, Alexei P.; Baron, Gregor; Zsurka, Gabor; Hampel, Kevin G.; Elger, Christian E.; Grote, Alexander; Weber, Yvonne; Lerche, Holger; Thiele, Holger; Nuernberg, Peter; Schulz, Herbert; Ruppert, Ann-Kathrin; Sander, Thomas; Cheng, Qing; Arner, Elias S. J.; Schomburg, Lutz; Seeher, Sandra; Fradejas-Villar, Noelia; Schweizer, Ulrich; Kunz, Wolfram S.

dc.contributor.author	Lerche, Holger
dc.contributor.author	Weber, Yvonne G.
dc.date.accessioned	2018-02-06T12:00:54Z
dc.date.available	2018-02-06T12:00:54Z
dc.date.issued	2017
dc.identifier.issn	1873-4596
dc.identifier.uri	http://hdl.handle.net/10900/80131
dc.language.iso	en	de_DE
dc.publisher	Elsevier Science Inc	de_DE
dc.relation.uri	http://dx.doi.org/10.1016/j.freeradbiomed.2017.02.040	de_DE
dc.rights	info:eu-repo/semantics/closedAccess
dc.subject.ddc	570	de_DE
dc.subject.ddc	610	de_DE
dc.title	Homozygous mutation in TXNRD1 is associated with genetic generalized epilepsy	de_DE
dc.type	Article	de_DE
utue.quellen.id	20170815222223_00925
utue.publikation.seiten	270-277	de_DE
utue.personen.roh	Kudin, Alexei P.
utue.personen.roh	Baron, Gregor
utue.personen.roh	Zsurka, Gabor
utue.personen.roh	Hampel, Kevin G.
utue.personen.roh	Elger, Christian E.
utue.personen.roh	Grote, Alexander
utue.personen.roh	Weber, Yvonne
utue.personen.roh	Lerche, Holger
utue.personen.roh	Thiele, Holger
utue.personen.roh	Nuernberg, Peter
utue.personen.roh	Schulz, Herbert
utue.personen.roh	Ruppert, Ann-Kathrin
utue.personen.roh	Sander, Thomas
utue.personen.roh	Cheng, Qing
utue.personen.roh	Arner, Elias S. J.
utue.personen.roh	Schomburg, Lutz
utue.personen.roh	Seeher, Sandra
utue.personen.roh	Fradejas-Villar, Noelia
utue.personen.roh	Schweizer, Ulrich
utue.personen.roh	Kunz, Wolfram S.
dcterms.isPartOf.ZSTitelID	Free Radical Biology and Medicine	de_DE
dcterms.isPartOf.ZS-Volume	106	de_DE
utue.fakultaet	04 Medizinische Fakultät	de_DE