umu.sePublications
Change search
CiteExportLink to record
Permanent link

Direct link
Cite
Citation style
  • apa
  • ieee
  • modern-language-association-8th-edition
  • vancouver
  • Other style
More styles
Language
  • de-DE
  • en-GB
  • en-US
  • fi-FI
  • nn-NO
  • nn-NB
  • sv-SE
  • Other locale
More languages
Output format
  • html
  • text
  • asciidoc
  • rtf
Reconsidering the causality of TIA1 mutations in ALS
Show others and affiliations
2018 (English)In: Amyotrophic Lateral Sclerosis and Frontotemporal Degeneration, ISSN 2167-8421, E-ISSN 2167-9223, Vol. 19, no 1-2, p. 1-3Article in journal, Editorial material (Other academic) Published
Place, publisher, year, edition, pages
TAYLOR & FRANCIS LTD , 2018. Vol. 19, no 1-2, p. 1-3
National Category
Neurosciences
Identifiers
URN: urn:nbn:se:umu:diva-145803DOI: 10.1080/21678421.2017.1413118ISI: 000425671500001PubMedID: 29235362Scopus ID: 2-s2.0-85038017115OAI: oai:DiVA.org:umu-145803DiVA, id: diva2:1238645
Available from: 2018-08-14 Created: 2018-08-14 Last updated: 2018-08-14Bibliographically approved

Open Access in DiVA

No full text in DiVA

Other links

Publisher's full textPubMedScopus

Authority records BETA

Andersen, Peter M.

Search in DiVA

By author/editor
Mclaughlin, Russell L.Andersen, Peter M.Hardiman, Orla
By organisation
Clinical Neuroscience
In the same journal
Amyotrophic Lateral Sclerosis and Frontotemporal Degeneration
Neurosciences

Search outside of DiVA

GoogleGoogle Scholar

doi
pubmed
urn-nbn

Altmetric score

doi
pubmed
urn-nbn
Total: 43 hits
CiteExportLink to record
Permanent link

Direct link
Cite
Citation style
  • apa
  • ieee
  • modern-language-association-8th-edition
  • vancouver
  • Other style
More styles
Language
  • de-DE
  • en-GB
  • en-US
  • fi-FI
  • nn-NO
  • nn-NB
  • sv-SE
  • Other locale
More languages
Output format
  • html
  • text
  • asciidoc
  • rtf