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AuthorLehmann-Horn, Frankdc.contributor.author
AuthorJurkat-Rott, K.dc.contributor.author
Date of accession2018-09-05T09:42:11Zdc.date.accessioned
Available in OPARU since2018-09-05T09:42:11Zdc.date.available
Date of first publication2011dc.date.issued
Languagededc.language.iso
PublisherUniversität Ulmdc.publisher
KeywordIon channelsdc.subject
Keywordmuscle disordersdc.subject
Keywordmuscle stiffnessdc.subject
Keywordmuscle weaknessdc.subject
Keywordmuscle degenerationdc.subject
Keywordmyotoniadc.subject
Keywordperiodic paralysisdc.subject
Keywordmalignant hyperthermiadc.subject
Keywordcore myopathydc.subject
Keywordhypokalemic periodic paralysisdc.subject
Keywordmalignant-hyperthermia susceptibilitydc.subject
Keywordpotassium-aggravated myotoniadc.subject
Keywordcalcium-channel mutationdc.subject
Keywordmulti-minicore diseasedc.subject
Keywordvitro contracture testdc.subject
Keywordskeletal-muscledc.subject
Keywordparamyotonia-congenitadc.subject
Keywordtransient weaknessdc.subject
Keywordcore myopathiesdc.subject
Dewey Decimal GroupDDC 610 / Medicine & healthdc.subject.ddc
TitleHereditary muscle channelopathiesdc.title
Resource typeWissenschaftlicher Artikeldc.type
FacultyMedizinische Fakultätuulm.affiliationGeneral
InstitutionInstitut für Angewandte Physiologieuulm.affiliationSpecific
DCMI TypeTextuulm.typeDCMI
CategoryPublikationsnachweiseuulm.category
Source - Title of sourceNervenheilkundesource.title
Source - Place of publicationSchattauersource.publisher
Source - Volume30source.volume
Source - Issue10source.issue
Source - Year2011source.year
Source - From page765+source.fromPage
Source - ISSN0722-1541source.identifier.issn
Open AccessNouulm.OA
CommunityMedizinische Fakultätuulm.community
WoS000296929700004uulm.identifier.wos
Bibliographyuulmuulm.bibliographie


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