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

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Title: Epilepsy subtype-specific copy number burden observed in a genome-wide study of 17 458 subjects.
Authors: Niestroj, Lisa-Marie1, Perez-Palma, Eduardo2, Howrigan, Daniel P3, Zhou, Yadi2, Cheng, Feixiong2,4,5, Saarentaus, Elmo6, Nürnberg, Peter1,7,8, Stevelink, Remi9,10, Daly, Mark J3,6,11, Palotie, Aarno3,6,11, Lal, Dennis1,2,3,12, lald@ccf.org, Collaborative, the Epi25, Epi25 Collaborative
Source: Brain: A Journal of Neurology; Jul2020, Vol. 143 Issue 7, p2106-2118, 13p
Database: Applied Science & Technology Source
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Header DbId: aci
DbLabel: Applied Science & Technology Source
An: 144668718
AccessLevel: 2
PubType: Academic Journal
PubTypeId: academicJournal
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        Value: 10.1093/brain/awaa171
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              Text: Jul2020
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