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AuthorMarroquin, Nicolaidc.contributor.author
AuthorStranz, Sebastiandc.contributor.author
AuthorMueller, Kathrindc.contributor.author
AuthorWieland, Thomasdc.contributor.author
AuthorRuf, Wolfgang P.dc.contributor.author
AuthorBrockmann, Sarah J.dc.contributor.author
AuthorDanzer, Karin M.dc.contributor.author
AuthorBorck, Guntramdc.contributor.author
AuthorHuebers, Annemariedc.contributor.author
AuthorWeydt, Patrickdc.contributor.author
AuthorMeitinger, Thomasdc.contributor.author
AuthorStrom, Tim-Matthiasdc.contributor.author
AuthorRosenbohm, Angeladc.contributor.author
AuthorLudolph, Albert C.dc.contributor.author
AuthorWeishaupt, Jochen H.dc.contributor.author
Date of accession2019-10-29T08:25:30Zdc.date.accessioned
Available in OPARU since2019-10-29T08:25:30Zdc.date.available
Date of first publication2016dc.date.issued
Languageendc.language.iso
PublisherUniversität Ulmdc.publisher
Dewey Decimal GroupDDC 610 / Medicine & healthdc.subject.ddc
TitleScreening for CHCHD10 mutations in a large cohort of sporadic ALS patients: no evidence for pathogenicity of the p.P34S variantdc.title
Resource typeWissenschaftlicher Artikeldc.type
InstitutionUKU. Klinik für Neurologieuulm.affiliationSpecific
InstitutionUKU. Institut für Humangenetikuulm.affiliationSpecific
DCMI TypeTextuulm.typeDCMI
CategoryPublikationsnachweiseuulm.category
DOI (external)10.1093/brain/awv218dc.identifier.doiExternal
Source - Title of sourceBrainsource.title
Source - Place of publicationOxford University Presssource.publisher
Source - Volume139source.volume
Source - Issue2source.issue
Source - Year2016source.year
Source - From pageE8source.fromPage
Source - To pageU10source.toPage
Source - ISSN0006-8950source.identifier.issn
Source - eISSN1460-2156source.identifier.eissn
Open AccessBronze, Green Publisheduulm.OA
CommunityUniversitätsklinikum Ulmuulm.community
WoS000370205100001uulm.identifier.wos
Bibliographyuulmuulm.bibliographie


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