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Ultra-Rare Genetic Variation in the Epilepsies: A Whole-Exome Sequencing Study of 17,606 Individuals.

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dc.contributor.authorEpi25, Collaborative.
dc.contributor.authorEpi25, Collaborative.
dc.contributor.institutionauthorYÜCESAN, EMRAH
dc.date.accessioned2020-01-14T21:00:27Z
dc.date.available2020-01-14T21:00:27Z
dc.date.issued2019-08-01T00:00:00Z
dc.identifier.citationEpi25 C., Epi25 C., -Ultra-Rare Genetic Variation in the Epilepsies: A Whole-Exome Sequencing Study of 17,606 Individuals.-, American journal of human genetics, cilt.105, ss.267-282, 2019
dc.identifier.doi10.1016/j.ajhg.2019.05.020
dc.identifier.pubmed31327507
dc.identifier.scopus85069831549
dc.identifier.urihttps://openaccess.bezmialem.edu.tr/handle/20.500.12645/12778
dc.identifier.wosWOS:000478022200004
dc.titleUltra-Rare Genetic Variation in the Epilepsies: A Whole-Exome Sequencing Study of 17,606 Individuals.
dc.typeArticle
dspace.entity.typePublication
local.avesis.id9527b08a-91e8-4fea-9a6c-59982d03ed42
local.indexed.atWOS
local.indexed.atScopus
local.publication.isinternational1
relation.isAuthorOfPublication9ea2b80f-531b-49a7-83ef-723bfd8584b2
relation.isAuthorOfPublication.latestForDiscovery9ea2b80f-531b-49a7-83ef-723bfd8584b2

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