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Exon-disrupting deletions of NRXN1 in idiopathic generalized epilepsy

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dc.contributor.authorTÜRKDOĞAN, DİLŞAD
dc.contributor.authorsMøller, Rikke S.; Weber, Yvonne G.; Klitten, Laura L.; Trucks, Holger; Muhle, Hiltrud; Kunz, Wolfram S.; Mefford, Heather C.; Franke, Andre; Kautza, Monika; Wolf, Peter; Dennig, Dieter; Schreiber, Stefan; Rückert, Ina-Maria; Wichmann, H.-Erich; Ernst, Jan P.; Schurmann, Claudia; Grabe, Hans J.; Tommerup, Niels; Stephani, Ulrich; Lerche, Holger; Hjalgrim, Helle; Helbig, Ingo; Sander, Thomas; EPICURE Consortium
dc.date.accessioned2022-03-02T05:37:38Z
dc.date.accessioned2026-01-10T20:49:59Z
dc.date.available2022-03-02T05:37:38Z
dc.date.issued2013-02
dc.identifier.doi10.1111/epi.12078
dc.identifier.issn139580
dc.identifier.issue2
dc.identifier.pages256-264
dc.identifier.urihttps://hdl.handle.net/11424/218406
dc.identifier.volume54
dc.language.isoeng
dc.relation.urihttps://onlinelibrary.wiley.com/doi/10.1111/epi.12078
dc.titleExon-disrupting deletions of NRXN1 in idiopathic generalized epilepsy
dc.typearticle
dspace.entity.typePublication

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