Senataxin helicase, the causal gene defect in ALS4, is a significant modifier of C9orf72 ALS G4C2 and arginine-containing dipeptide repeat toxicity

Location
Deutsche Nationalbibliothek Frankfurt am Main
Extent
1 Online-Ressource.
Language
Englisch

Bibliographic citation
Senataxin helicase, the causal gene defect in ALS4, is a significant modifier of C9orf72 ALS G4C2 and arginine-containing dipeptide repeat toxicity ; volume:11 ; number:1 ; day:17 ; month:10 ; year:2023 ; pages:1-18 ; date:12.2023
Acta Neuropathologica Communications ; 11, Heft 1 (17.10.2023), 1-18, 12.2023

Creator
Bennett, Craig L.
Dastidar, Somasish
Arnold, Frederick J.
McKinstry, Spencer U.
Stockford, Cameron
Freibaum, Brian D.
Sopher, Bryce L.
Wu, Meilin
Seidner, Glen
Joiner, William
Taylor, J. Paul
West, Ryan J. H.
Spada, Albert R. La
Contributor
SpringerLink (Online service)

DOI
10.1186/s40478-023-01665-z
URN
urn:nbn:de:101:1-2024020710381583478544
Rights
Open Access; Der Zugriff auf das Objekt ist unbeschränkt möglich.
Last update
15.08.2025, 7:29 AM CEST

Data provider

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Associated

  • Bennett, Craig L.
  • Dastidar, Somasish
  • Arnold, Frederick J.
  • McKinstry, Spencer U.
  • Stockford, Cameron
  • Freibaum, Brian D.
  • Sopher, Bryce L.
  • Wu, Meilin
  • Seidner, Glen
  • Joiner, William
  • Taylor, J. Paul
  • West, Ryan J. H.
  • Spada, Albert R. La
  • SpringerLink (Online service)

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