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Epilepsy subtype-specific copy number burden observed in a genome-wide study of 17 458 subjects.

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dc.contributor.authorNiestroj, LM
dc.contributor.authorPerez-Palma, E
dc.contributor.authorHowrigan, DP
dc.contributor.authorZhou, Y
dc.contributor.authorCheng, F
dc.contributor.authorSaarentaus, E
dc.contributor.authorNürnberg, P
dc.contributor.authorStevelink, R
dc.contributor.authorDaly, MJ
dc.contributor.authorPalotie, A
dc.contributor.authorLal, D
dc.contributor.authorEpi25, Collaborative
dc.contributor.institutionauthorYÜCESAN, EMRAH
dc.date.accessioned2020-08-31T20:59:17Z
dc.date.available2020-08-31T20:59:17Z
dc.date.issued2020-07-01T00:00:00Z
dc.identifier.citationNiestroj L., Perez-Palma E., Howrigan D., Zhou Y., Cheng F., Saarentaus E., Nürnberg P., Stevelink R., Daly M., Palotie A., et al., -Epilepsy subtype-specific copy number burden observed in a genome-wide study of 17 458 subjects.-, Brain : a journal of neurology, cilt.143, ss.2106-2118, 2020
dc.identifier.doi10.1093/brain/awaa171
dc.identifier.scopus85088262031
dc.identifier.urihttp://hdl.handle.net/20.500.12645/18473
dc.language.isoen
dc.titleEpilepsy subtype-specific copy number burden observed in a genome-wide study of 17 458 subjects.
dc.typeArticle
dspace.entity.typePublication
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local.indexed.atScopus
local.publication.goal03 - Sağlık ve Kaliteli Yaşam
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relation.isGoalOfPublication9c198c48-b603-4e2f-8366-04edcfc1224c
relation.isGoalOfPublication.latestForDiscovery9c198c48-b603-4e2f-8366-04edcfc1224c

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