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AuthorZielonka, Danieldc.contributor.author
AuthorJurkat-Rott, Karindc.contributor.author
AuthorStachowiak, Paweldc.contributor.author
AuthorBryl, Annadc.contributor.author
AuthorMarcinkowski, Jerzy T.dc.contributor.author
AuthorLehmann-Horn, Frankdc.contributor.author
Date of accession2018-08-13T07:28:00Zdc.date.accessioned
Available in OPARU since2018-08-13T07:28:00Zdc.date.available
Date of first publication2012dc.date.issued
Languageendc.language.iso
PublisherUniversität Ulmdc.publisher
KeywordChloride channel myotoniadc.subject
KeywordCLCN1-MLPAdc.subject
KeywordPrinzmetal anginadc.subject
Keywordmuscle chloride channeldc.subject
Keywordcongenitadc.subject
Keywordgenedc.subject
Keywordinvolvementdc.subject
Keywordphenotypedc.subject
Keyworddominantdc.subject
Keywordlipomasdc.subject
Dewey Decimal GroupDDC 610 / Medicine & healthdc.subject.ddc
TitleA Becker myotonia patient with compound heterozygosity for CLCN1 mutations and Prinzmetal angina pectorisdc.title
Resource typeWissenschaftlicher Artikeldc.type
InstitutionUKU. Klinik für Neurologieuulm.affiliationSpecific
InstitutionNeurophysiologieuulm.affiliationSpecific
DCMI TypeTextuulm.typeDCMI
CategoryPublikationsnachweiseuulm.category
DOI (external)10.1016/j.nmd.2011.10.024dc.identifier.doiExternal
Source - Title of sourceNeuromuscular Disorderssource.title
Source - Place of publicationElseviersource.publisher
Source - Volume22source.volume
Source - Issue4source.issue
Source - Year2012source.year
Source - From page355source.fromPage
Source - To page360source.toPage
Source - ISSN0960-8966source.identifier.issn
Open AccessNouulm.OA
Suitable communityUniversitätsklinikum Ulmuulm.community
WoS000303143500008uulm.identifier.wos
University Bibliographyjauulm.unibibliographie


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