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AuthorFan, C.dc.contributor.author
AuthorMao, N.dc.contributor.author
AuthorLehmann-Horn, Frankdc.contributor.author
AuthorBuermann, J.dc.contributor.author
AuthorJurkat-Rott, K.dc.contributor.author
Date of accession2018-09-06T09:40:06Zdc.date.accessioned
Available in OPARU since2018-09-06T09:40:06Zdc.date.available
Date of first publication2017dc.date.issued
Languageendc.language.iso
PublisherUniversität Ulmdc.publisher
Keywordfounder effectdc.subject
Keywordhyperkalemic periodic paralysisdc.subject
KeywordNa(v)1dc.subject
Keyword4dc.subject
Keywordnovel borderline mutationdc.subject
Keywordimpaired slow inactivationdc.subject
Keywordgated sodium-channelsdc.subject
Keywordna+ channeldc.subject
Keywordfunctional expressiondc.subject
Keywordmuscledc.subject
Keywordexcitabilitydc.subject
Keywordactivationdc.subject
Keywordphenotypedc.subject
Keywordmechanismdc.subject
Keywordgenotypedc.subject
Dewey Decimal GroupDDC 610 / Medicine & healthdc.subject.ddc
TitleEffects of S906T polymorphism on the severity of a novel borderline mutation I692M in Na(v)1.4 cause periodic paralysisdc.title
Resource typeWissenschaftlicher Artikeldc.type
InstitutionUKU. Klinik für Neurochirurgieuulm.affiliationSpecific
InstitutionUKU. Klinik für Neurologieuulm.affiliationSpecific
InstitutionNeurophysiologieuulm.affiliationSpecific
DCMI TypeTextuulm.typeDCMI
CategoryPublikationsnachweiseuulm.category
DOI (external)10.1111/cge.12880dc.identifier.doiExternal
Source - Title of sourceClinical Geneticssource.title
Source - Place of publicationWileysource.publisher
Source - Volume91source.volume
Source - Issue6source.issue
Source - Year2017source.year
Source - From page859source.fromPage
Source - To page867source.toPage
Source - ISSN0009-9163source.identifier.issn
Source - eISSN1399-0004source.identifier.eissn
Open AccessNouulm.OA
CommunityUniversitätsklinikum Ulmuulm.community
WoS000402143900007uulm.identifier.wos
Bibliographyuulmuulm.bibliographie


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