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Exon-disrupting deletions of NRXN1 in idiopathic generalized epilepsy.

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dc.contributor.authorMøller, RS
dc.contributor.authorWeber, YG
dc.contributor.authorKlitten, LL
dc.contributor.authorTrucks, H
dc.contributor.authorMuhle, H
dc.contributor.authorKunz, WS
dc.contributor.authorMefford, HC
dc.contributor.authorFranke, A
dc.contributor.authorKautza, M
dc.contributor.authorWolf, P
dc.contributor.authorDennig, D
dc.contributor.authorSchreiber, S
dc.contributor.authorRückert, IM
dc.contributor.authorWichmann, HE
dc.contributor.authorErnst, JP
dc.contributor.authorSchurmann, C
dc.contributor.authorGrabe, HJ
dc.contributor.authorTommerup, N
dc.contributor.authorStephani, U
dc.contributor.authorLerche, H
dc.contributor.authorHjalgrim, H
dc.contributor.authorHelbig, I
dc.contributor.authorSander, T
dc.contributor.authorEPICURE, Consortium.
dc.contributor.institutionauthorYÜCESAN, EMRAH
dc.date.accessioned2020-01-14T21:00:31Z
dc.date.available2020-01-14T21:00:31Z
dc.date.issued2013-02-01T00:00:00Z
dc.identifier.citationMøller R., Weber Y., Klitten L., Trucks H., Muhle H., Kunz W., Mefford H., Franke A., Kautza M., Wolf P., et al., -Exon-disrupting deletions of NRXN1 in idiopathic generalized epilepsy.-, Epilepsia, cilt.54, ss.256-64, 2013
dc.identifier.doi10.1111/epi.12078
dc.identifier.scopus84978024392
dc.identifier.urihttps://openaccess.bezmialem.edu.tr/handle/20.500.12645/12782
dc.identifier.wosWOS:000314750200008
dc.titleExon-disrupting deletions of NRXN1 in idiopathic generalized epilepsy.
dc.typeArticle
dspace.entity.typePublication
local.avesis.id9a2956a5-d08e-4f28-bb53-8313fc8dd81d
local.publication.isinternational1
relation.isAuthorOfPublication9ea2b80f-531b-49a7-83ef-723bfd8584b2
relation.isAuthorOfPublication.latestForDiscovery9ea2b80f-531b-49a7-83ef-723bfd8584b2
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