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AuthorKreppel, Floriandc.contributor.author
Date of accession2020-08-18T04:51:48Zdc.date.accessioned
Available in OPARU since2020-08-18T04:51:48Zdc.date.available
Date of first publication2010dc.date.issued
Languageendc.language.iso
PublisherUniversität Ulmdc.publisher
KeywordSEVERE COMBINED IMMUNODEFICIENCYdc.subject
KeywordCHRONIC GRANULOMATOUS-DISEASEdc.subject
KeywordLEBERS CONGENITAL AMAUROSISdc.subject
KeywordADENOASSOCIATED VIRUSdc.subject
KeywordIMMUNE-RESPONSEdc.subject
KeywordSCID-X1dc.subject
KeywordMUTATIONSdc.subject
KeywordADAdc.subject
Dewey Decimal GroupDDC 610 / Medicine & healthdc.subject.ddc
TitleAAV-2: how can the capsid be modified to improve the viral vector in gene therapy?dc.title
Resource typeWissenschaftlicher Artikeldc.type
InstitutionUKU. Abteilung für Gentherapieuulm.affiliationSpecific
DCMI TypeTextuulm.typeDCMI
CategoryPublikationsnachweiseuulm.category
DOI (external)10.2217/FVL.10.6dc.identifier.doiExternal
Source - Title of sourceFuture virologysource.title
Source - Place of publicationFuture Medicine Ltdsource.publisher
Source - Volume5source.volume
Source - Issue2source.issue
Source - Year2010source.year
Source - From page133source.fromPage
Source - To page135source.toPage
Source - ISSN1746-0794source.identifier.issn
Source - eISSN1746-0808source.identifier.eissn
Suitable communityUniversitätsklinikum Ulmuulm.community
WoS000275779200002uulm.identifier.wos
University Bibliographyjauulm.unibibliographie


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