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AuthorSpeckmann, Carstendc.contributor.author
AuthorSahoo, Sushree Sangitadc.contributor.author
AuthorRizzi, Martadc.contributor.author
AuthorHirabayashi, Shinsukedc.contributor.author
AuthorKarow, Axeldc.contributor.author
AuthorSerwas, Nina Kathrindc.contributor.author
AuthorHoemberg, Marcdc.contributor.author
AuthorDamatova, Nataljadc.contributor.author
AuthorSchindler, Detlevdc.contributor.author
AuthorVannier, Jean-Baptistedc.contributor.author
AuthorBoulton, Simon J.dc.contributor.author
AuthorPannicke, Ulrichdc.contributor.author
AuthorGoehring, Gudrundc.contributor.author
AuthorThomay, Kathrindc.contributor.author
AuthorVerdu-Amoros, J. J.dc.contributor.author
AuthorHauch, Holgerdc.contributor.author
AuthorWoessmann, Wilhelmdc.contributor.author
AuthorEscherich, Gabrieledc.contributor.author
AuthorLaack, Eckartdc.contributor.author
AuthorRindle, Lilianadc.contributor.author
AuthorSeidl, Maximiliandc.contributor.author
AuthorRensing-Ehl, Annedc.contributor.author
AuthorLausch, Ekkehartdc.contributor.author
AuthorJandrasits, Christinedc.contributor.author
AuthorStrahm, Brigittedc.contributor.author
AuthorSchwarz, Klausdc.contributor.author
AuthorEhl, Stephan R.dc.contributor.author
AuthorNiemeyer, Charlottedc.contributor.author
AuthorBoztug, Kaandc.contributor.author
AuthorWlodarski, Marcin W.dc.contributor.author
Date of accession2019-01-25T09:42:08Zdc.date.accessioned
Available in OPARU since2019-01-25T09:42:08Zdc.date.available
Date of first publication2017dc.date.issued
Languageendc.language.iso
PublisherUniversität Ulmdc.publisher
KeywordRTEL1dc.subject
Keyworddyskeratosis congenitadc.subject
Keywordbone marrow failuredc.subject
Keywordimmunodeficiencydc.subject
Keywordlymphopeniadc.subject
Keywordhoyeraal-hreidarsson syndromedc.subject
Keywordfamilial pulmonary-fibrosisdc.subject
Keyworddna-sequencing datadc.subject
Keyworddyskeratosis-congenitadc.subject
Keywordcombined immunodeficiencydc.subject
Keywordhomologous recombinationdc.subject
Keywordtelomere maintenancedc.subject
Keywordgenetic featuresdc.subject
Keywordmutationsdc.subject
Keywordhelicasedc.subject
Dewey Decimal GroupDDC 610 / Medicine & healthdc.subject.ddc
TitleClinical and Molecular Heterogeneity of RTEL1 Deficiencydc.title
Resource typeWissenschaftlicher Artikeldc.type
InstitutionInstitut für Klinische Transfusionsmedizin und Immungenetik Ulm gGmbH (IKT)uulm.affiliationSpecific
DCMI TypeTextuulm.typeDCMI
CategoryPublikationsnachweiseuulm.category
DOI (external)10.3389/fimmu.2017.00449dc.identifier.doiExternal
Source - Title of sourceFrontiers in Immunologysource.title
Source - Place of publicationFrontiers Mediasource.publisher
Source - Volume8source.volume
Source - Year2017source.year
Source - Article number449source.articleNumber
Source - ISSN1664-3224source.identifier.issn
Open Accessgolduulm.OA
CommunityWeitere Einrichtungenuulm.community
WoS000400317500001uulm.identifier.wos
Bibliographyuulmuulm.bibliographie


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