Publication:
Familial and sporadic 15q13.3 microdeletions in idiopathic generalized epilepsy: precedent for disorders with complex inheritance

dc.contributor.authorTÜRKDOĞAN, DİLŞAD
dc.contributor.authorsDibbens, L. M.; Mullen, S.; Helbig, I.; Mefford, H. C.; Bayly, M. A.; Bellows, S.; Leu, C.; Trucks, H.; Obermeier, T.; Wittig, M.; Franke, A.; Caglayan, H.; Yapici, Z.; EPICURE Consortium; Sander, T.; Eichler, E. E.; Scheffer, I. E.; Mulley, J. C.; Berkovic, S. F.
dc.date.accessioned2022-03-02T05:36:22Z
dc.date.available2022-03-02T05:36:22Z
dc.date.issued2009-10-01
dc.identifier.doi10.1093/hmg/ddp311
dc.identifier.issn0964-6906, 1460-2083
dc.identifier.issue19
dc.identifier.pages3626-3631
dc.identifier.urihttps://hdl.handle.net/11424/218281
dc.identifier.volume18
dc.language.isoeng
dc.relation.urihttps://academic.oup.com/hmg/article-lookup/doi/10.1093/hmg/ddp311
dc.titleFamilial and sporadic 15q13.3 microdeletions in idiopathic generalized epilepsy: precedent for disorders with complex inheritance
dc.title.alternativeFamilial and sporadic 15q13.3 microdeletions in idiopathic generalized epilepsy
dc.typearticle
dspace.entity.typePublication
local.avesis.idc61331a2-b32e-42c1-9b1a-3951830931fe
local.indexed.atSCOPUS
relation.isAuthorOfPublication0a1599c4-48ff-4aa9-b689-3927c986a650
relation.isAuthorOfPublication.latestForDiscovery0a1599c4-48ff-4aa9-b689-3927c986a650

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