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AuthorJurkat-Rott, Karindc.contributor.author
AuthorLehmann-Horn, Frankdc.contributor.author
Date of accession2018-09-06T07:56:01Zdc.date.accessioned
Available in OPARU since2018-09-06T07:56:01Zdc.date.available
Date of first publication2007dc.date.issued
Languageendc.language.iso
PublisherUniversität Ulmdc.publisher
Keywordhyperkalemic periodic paralysisdc.subject
Keywordmyotoniadc.subject
Keywordhypokalemic periodic paralysisdc.subject
KeywordAndersen-Tawil syndromedc.subject
Keywordvoltage-gated sodium channeldc.subject
Keywordchannelopathiesdc.subject
Keywordmuscle sodium-channeldc.subject
Keywordadynamia episodica hereditariadc.subject
Keywordparamyotonia-congenitadc.subject
Keywordskeletal-muscledc.subject
Keywordandersens-syndromedc.subject
Keywordslow inactivationdc.subject
Keywordalpha-subunitdc.subject
Keywordcardiac-arrhythmiadc.subject
Keywordkcnj2 mutationsdc.subject
Dewey Decimal GroupDDC 610 / Medicine & healthdc.subject.ddc
TitleGenotype-phenotype correlation and therapeutic rationale in Hyperkalemic periodic paralysisdc.title
Resource typeWissenschaftlicher Artikeldc.type
FacultyMedizinische Fakultätuulm.affiliationGeneral
InstitutionInstitut für Angewandte Physiologieuulm.affiliationSpecific
DCMI TypeTextuulm.typeDCMI
CategoryPublikationsnachweiseuulm.category
DOI (external)10.1016/j.nurt.2007.02.001dc.identifier.doiExternal
Source - Title of sourceNeurotherapeuticssource.title
Source - Place of publicationElsevier Sciencesource.publisher
Source - Volume4source.volume
Source - Issue2source.issue
Source - Year2007source.year
Source - From page216source.fromPage
Source - To page224source.toPage
Source - ISSN1933-7213source.identifier.issn
Open AccessNouulm.OA
CommunityMedizinische Fakultätuulm.community
WoS000249762700006uulm.identifier.wos
Bibliographyuulmuulm.bibliographie


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