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AuthorKarges, Bdc.contributor.author
AuthorKrause, Gdc.contributor.author
AuthorHomoki, Jdc.contributor.author
AuthorDebatin, Klaus-Michaeldc.contributor.author
Authorde Roux, Ndc.contributor.author
AuthorKarges, Wdc.contributor.author
Date of accession2018-06-14T08:55:47Zdc.date.accessioned
Available in OPARU since2018-06-14T08:55:47Zdc.date.available
Date of first publication2005dc.date.issued
Languageendc.language.iso
PublisherUniversität Ulmdc.publisher
Keywordstimulating hormone-receptordc.subject
Keywordhuman thyrotropin receptordc.subject
Keywordprotein-coupled receptorsdc.subject
Keywordhyperfunctioning thyroid adenomasdc.subject
Keywordactivating mutationdc.subject
Keywordgermline mutationsdc.subject
Keywordcongenital hyperthyroidismdc.subject
Keywordinactive conformationdc.subject
Keywordsomatic mutationsdc.subject
Keywordgenedc.subject
Dewey Decimal GroupDDC 610 / Medicine & healthdc.subject.ddc
TitleTSH receptor mutation V509A causes familial hyperthyroidism by release of interhelical constraints between transmembrane helices TMH3 and TMH5dc.title
Resource typeWissenschaftlicher Artikeldc.type
InstitutionUKU. Klinik für Kinder- und Jugendmedizinuulm.affiliationSpecific
InstitutionUKU. Klinik für Innere Medizin Iuulm.affiliationSpecific
DCMI TypeTextuulm.typeDCMI
CategoryPublikationsnachweiseuulm.category
DOI (external)10.1677/joe.1.06208dc.identifier.doiExternal
Source - Title of sourceJournal of Endocrinologysource.title
Source - Place of publicationSociety for Endocrinologysource.publisher
Source - Volume186source.volume
Source - Issue2source.issue
Source - Year2005source.year
Source - From page377source.fromPage
Source - To page385source.toPage
Source - ISSN0022-0795source.identifier.issn
Open AccessNouulm.OA
CommunityUniversitätsklinikum Ulmuulm.community
WoS000231706900011uulm.identifier.wos
Bibliographyuulmuulm.bibliographie


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