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AuthorNonnenmacher, L.dc.contributor.author
AuthorLanger, T.dc.contributor.author
AuthorBlessing, H.dc.contributor.author
AuthorGabriel, H.dc.contributor.author
AuthorBuchwald, H. J.dc.contributor.author
AuthorMeneksedag, C.dc.contributor.author
AuthorKohne, E.dc.contributor.author
AuthorGencik, M.dc.contributor.author
AuthorDebatin, Klaus-Michaeldc.contributor.author
AuthorCario, H.dc.contributor.author
Date of accession2018-06-12T08:48:23Zdc.date.accessioned
Available in OPARU since2018-06-12T08:48:23Zdc.date.available
Date of first publication2011dc.date.issued
Languageendc.language.iso
PublisherUniversität Ulmdc.publisher
Keywordhereditary hyperferritinemia cataract syndromedc.subject
KeywordFTL genedc.subject
Keywordearly onset cataractdc.subject
Keywordhyperferritinemiadc.subject
KeywordHHCSdc.subject
Keywordiron-responsive elementdc.subject
Keywordl-ferritindc.subject
Keywordmutationsdc.subject
Keyworddiagnosisdc.subject
Keywordoverloaddc.subject
Keywordhemochromatosisdc.subject
Keywordidentificationdc.subject
Keywordchaindc.subject
Dewey Decimal GroupDDC 610 / Medicine & healthdc.subject.ddc
TitleHereditary Hyperferritinemia Cataract Syndrome: Clinical, Genetic, and Laboratory Findings in 5 Familiesdc.title
Resource typeWissenschaftlicher Artikeldc.type
InstitutionUKU. Klinik für Kinder- und Jugendmedizinuulm.affiliationSpecific
InstitutionUKU. Klinik für Augenheilkundeuulm.affiliationSpecific
DCMI TypeTextuulm.typeDCMI
CategoryPublikationsnachweiseuulm.category
DOI (external)10.1055/s-0031-1287825dc.identifier.doiExternal
Source - Title of sourceKlinische Pädiatriesource.title
Source - Place of publicationGeorg Thieme Verlagsource.publisher
Source - Volume223source.volume
Source - Issue6source.issue
Source - Year2011source.year
Source - From page346source.fromPage
Source - To page351source.toPage
Source - ISSN0300-8630source.identifier.issn
Open AccessNouulm.OA
Suitable communityUniversitätsklinikum Ulmuulm.community
WoS000298060700008uulm.identifier.wos
University Bibliographyjauulm.unibibliographie


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