Senataxin helicase, the causal gene defect in ALS4, is a significant modifier of C9orf72 ALS G4C2 and arginine-containing dipeptide repeat toxicity
- Location
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Deutsche Nationalbibliothek Frankfurt am Main
- Extent
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1 Online-Ressource.
- Language
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Englisch
- Bibliographic citation
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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
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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
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SpringerLink (Online service)
- DOI
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10.1186/s40478-023-01665-z
- URN
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urn:nbn:de:101:1-2024020710381583478544
- Rights
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Open Access; Der Zugriff auf das Objekt ist unbeschränkt möglich.
- Last update
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15.08.2025, 7:29 AM CEST
Data provider
Deutsche Nationalbibliothek. If you have any questions about the object, please contact the data provider.
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)