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

dc.contributor.author	Daly, MJ
dc.contributor.author	Epi25, Collaborative
dc.contributor.author	Lal, D
dc.contributor.author	Stevelink, R
dc.contributor.author	Palotie, A
dc.contributor.author	Niestroj, LM
dc.contributor.author	Perez-Palma, E
dc.contributor.author	Howrigan, DP
dc.contributor.author	Zhou, Y
dc.contributor.author	Cheng, F
dc.contributor.author	Saarentaus, E
dc.contributor.author	Nürnberg, P
dc.date.accessioned	2021-03-03T17:30:00Z
dc.date.available	2021-03-03T17:30:00Z
dc.identifier.citation	Niestroj 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.issn	0006-8950
dc.identifier.other	vv_1032021
dc.identifier.other	av_4a0b4b07-c0dd-4da5-ac91-d69df820e832
dc.identifier.uri	http://hdl.handle.net/20.500.12627/53208
dc.identifier.uri	https://doi.org/10.1093/brain/awaa171
dc.language.iso	eng
dc.title	Epilepsy subtype-specific copy number burden observed in a genome-wide study of 17 458 subjects.
dc.type	Makale
dc.relation.journal	Brain : a journal of neurology
dc.contributor.department	, ,
dc.identifier.volume	143
dc.identifier.startpage	2106
dc.identifier.endpage	2118
dc.contributor.firstauthorID	2207715

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