Show simple item record

Authorvan Doormaal, Perry T. C.dc.contributor.author
AuthorTicozzi, Nicoladc.contributor.author
AuthorWeishaupt, Jochen H.dc.contributor.author
AuthorKenna, Kevindc.contributor.author
AuthorDiekstra, Frank P.dc.contributor.author
AuthorVerde, Federicodc.contributor.author
AuthorAndersen, Peter M.dc.contributor.author
AuthorDekker, Annelot M.dc.contributor.author
AuthorTiloca, Cinziadc.contributor.author
AuthorMarroquin, Nicolaidc.contributor.author
AuthorOverste, Daniel J.dc.contributor.author
AuthorPensato, Vivianadc.contributor.author
AuthorNuernberg, Peterdc.contributor.author
AuthorPulit, Sara L.dc.contributor.author
AuthorSchellevis, Raymond D.dc.contributor.author
AuthorCalini, Danieladc.contributor.author
AuthorAltmueller, Janinedc.contributor.author
AuthorFrancioli, Laurent C.dc.contributor.author
AuthorMuller, Bernarddc.contributor.author
AuthorCastellotti, Barbaradc.contributor.author
AuthorMotameny, Susannedc.contributor.author
AuthorRatti, Antoniadc.contributor.author
AuthorWolf, Joachimdc.contributor.author
AuthorGellera, Cinziadc.contributor.author
AuthorLudolph, Albert C.dc.contributor.author
Authorvan den Berg, Leonard H.dc.contributor.author
AuthorKubisch, Christiandc.contributor.author
AuthorLanders, John E.dc.contributor.author
AuthorVeldink, Jan H.dc.contributor.author
AuthorSilani, Vincenzodc.contributor.author
AuthorVolk, Alexander E.dc.contributor.author
Date of accession2018-12-07T05:38:18Zdc.date.accessioned
Available in OPARU since2018-12-07T05:38:18Zdc.date.available
Date of first publication2017dc.date.issued
Languageendc.language.iso
PublisherUniversität Ulmdc.publisher
KeywordALSdc.subject
Keywordamyotrophic lateral sclerosisdc.subject
Keywordde novo mutationsdc.subject
Keyworddisease pathwaydc.subject
Keywordmotor neuron diseasedc.subject
Keywordtriosdc.subject
Keywordfamilial alsdc.subject
Keywordsporadic alsdc.subject
Keywordvariantsdc.subject
Keyworddiseasedc.subject
Keywordpopulationdc.subject
Keywordpatternsdc.subject
Keywordriskdc.subject
Keywordagedc.subject
Dewey Decimal GroupDDC 610 / Medicine & healthdc.subject.ddc
TitleThe role of de novo mutations in the development of amyotrophic lateral sclerosisdc.title
Resource typeWissenschaftlicher Artikeldc.type
InstitutionUKU. Klinik für Neurologieuulm.affiliationSpecific
InstitutionUKU. Institut für Humangenetikuulm.affiliationSpecific
DCMI TypeTextuulm.typeDCMI
CategoryPublikationsnachweiseuulm.category
DOI (external)10.1002/humu.23295dc.identifier.doiExternal
Source - Title of sourceHuman Mutationsource.title
Source - Place of publicationWileysource.publisher
Source - Volume38source.volume
Source - Issue11source.issue
Source - Year2017source.year
Source - From page1534source.fromPage
Source - To page1541source.toPage
Source - ISSN1059-7794source.identifier.issn
Source - eISSN1098-1004source.identifier.eissn
CommunityUniversitätsklinikum Ulmuulm.community
WoS000412835700011uulm.identifier.wos
Bibliographyuulmuulm.bibliographie
Project uulmIGradU / International Graduate School der Universität Ulmuulm.projectOther


Files in this item

FilesSizeFormatView

There are no files associated with this item.

This item appears in the following Collection(s)

Show simple item record