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Choline transporter mutations in severe congenital myasthenic syndrome disrupt transporter localization

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dc.contributor.authorWang, HC
dc.contributor.authorSalter, CG
dc.contributor.authorRefai, O
dc.contributor.authorHardy, H
dc.contributor.authorBarwick, KES
dc.contributor.authorAkpulat, U
dc.contributor.authorKvarnung, M
dc.contributor.authorChioza, BA
dc.contributor.authorHarlalka, G
dc.contributor.authorTaylan, F
dc.contributor.authorSejersen, T
dc.contributor.authorWright, J
dc.contributor.authorZimmerman, HH
dc.contributor.authorKarakaya, M
dc.contributor.authorStuve, B
dc.contributor.authorWeis, J
dc.contributor.authorSchara, U
dc.contributor.authorRussell, MA
dc.contributor.authorAbdul-Rahman, OA
dc.contributor.authorChilton, J
dc.contributor.authorBlakely, RD
dc.contributor.authorBaple, EL
dc.contributor.authorCirak, S
dc.contributor.authorCrosby, AH
dc.date.accessioned2023-04-18T02:32:19Z
dc.date.available2023-04-18T02:32:19Z
dc.date.issued2017.01.01
dc.identifier.doi10.1093/brain/awx249
dc.identifier.eissn1460-2156
dc.identifier.endpage2850
dc.identifier.issn0006-8950
dc.identifier.issue
dc.identifier.startpage2838
dc.identifier.urihttps://www.webofscience.com/api/gateway?GWVersion=2&SrcApp=dspace_ku&SrcAuth=WosAPI&KeyUT=WOS:000414357800016&DestLinkType=FullRecord&DestApp=WOS
dc.identifier.urihttps://hdl.handle.net/20.500.12597/9726
dc.identifier.volume140
dc.identifier.wosWOS:000414357800016
dc.relation.ispartofBRAIN
dc.titleCholine transporter mutations in severe congenital myasthenic syndrome disrupt transporter localization
dc.typeArticle
dspace.entity.typeWos
relation.isPublicationOfWosd92120c4-5e95-4733-81e0-b2dd981c2b92
relation.isPublicationOfWos.latestForDiscoveryd92120c4-5e95-4733-81e0-b2dd981c2b92

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