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The SCN8A encephalopathy mutation p.Ile1327Val displays elevated sensitivity to the anticonvulsant phenytoin
dc.contributor.authorBarker, Bryan S.
dc.contributor.authorOttolini, Matteo
dc.contributor.authorWagnon, Jacy L.
dc.contributor.authorHollander, Rachel M.
dc.contributor.authorMeisler, Miriam H.
dc.contributor.authorPatel, Manoj K.
dc.date.accessioned2016-10-17T21:20:40Z
dc.date.available2017-11-01T15:31:30Zen
dc.date.issued2016-09
dc.identifier.citationBarker, Bryan S.; Ottolini, Matteo; Wagnon, Jacy L.; Hollander, Rachel M.; Meisler, Miriam H.; Patel, Manoj K. (2016). "The SCN8A encephalopathy mutation p.Ile1327Val displays elevated sensitivity to the anticonvulsant phenytoin." Epilepsia (9): 1458-1466.
dc.identifier.issn0013-9580
dc.identifier.issn1528-1167
dc.identifier.urihttps://hdl.handle.net/2027.42/134291
dc.publisherWiley Periodicals, Inc.
dc.subject.otherPhenytoin
dc.subject.otherSCN8A
dc.subject.otherAnticonvulsant drugs
dc.subject.otherSodium channels
dc.subject.otherEpileptic encephalopathy
dc.titleThe SCN8A encephalopathy mutation p.Ile1327Val displays elevated sensitivity to the anticonvulsant phenytoin
dc.typeArticleen_US
dc.rights.robotsIndexNoFollow
dc.subject.hlbsecondlevelMedicine (General)
dc.subject.hlbtoplevelHealth Sciences
dc.description.peerreviewedPeer Reviewed
dc.description.bitstreamurlhttp://deepblue.lib.umich.edu/bitstream/2027.42/134291/1/epi13461_am.pdf
dc.description.bitstreamurlhttp://deepblue.lib.umich.edu/bitstream/2027.42/134291/2/epi13461.pdf
dc.identifier.doi10.1111/epi.13461
dc.identifier.sourceEpilepsia
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dc.owningcollnameInterdisciplinary and Peer-Reviewed


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