SPG7 mutations in amyotrophic lateral sclerosis: a genetic link to hereditary spastic paraplegia
- Location
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Deutsche Nationalbibliothek Frankfurt am Main
- ISSN
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1432-1459
- Extent
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Online-Ressource
- Language
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Englisch
- Notes
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online resource.
- Bibliographic citation
-
SPG7 mutations in amyotrophic lateral sclerosis: a genetic link to hereditary spastic paraplegia ; day:23 ; month:5 ; year:2020 ; pages:1-12
Journal of neurology ; (23.5.2020), 1-12
- Creator
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Osmanovic, Alma
Widjaja, Maylin
Förster, Alisa
Weder, Julia
Wattjes, Mike P.
Lange, Inken
Sarikidi, Anastasia
Auber, Bernd
Raab, Peter
Christians, Anne
Preller, Matthias
Petri, Susanne
Weber, Ruthild G.
- Contributor
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SpringerLink (Online service)
- DOI
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10.1007/s00415-020-09861-w
- URN
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urn:nbn:de:101:1-2020072905001663469748
- Rights
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Open Access; Der Zugriff auf das Objekt ist unbeschränkt möglich.
- Last update
-
14.08.2025, 11:01 AM CEST
Data provider
This object is provided by:
Deutsche Nationalbibliothek. If you have any questions about the object, please contact the data provider.
Deutsche Nationalbibliothek. If you have any questions about the object, please contact the data provider.
Associated
- Osmanovic, Alma
- Widjaja, Maylin
- Förster, Alisa
- Weder, Julia
- Wattjes, Mike P.
- Lange, Inken
- Sarikidi, Anastasia
- Auber, Bernd
- Raab, Peter
- Christians, Anne
- Preller, Matthias
- Petri, Susanne
- Weber, Ruthild G.
- SpringerLink (Online service)
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Neuroinflammatory disease signatures in SPG11-related hereditary spastic paraplegia patients
The role of inflammation in hereditary spastic paraplegia type 11
Hereditary spastic paraplegia from 1880 to 2017: an historical review
Non-pharmacological treatment of hereditary spastic paraplegia: a systematic review
Functional characterization of hereditary spastic paraplegia proteins spastin and ZFYVE27
Gene identification in Hereditary Spastic Paraplegias and characterization of Spastic Paraplegia type 58 (SPG58)
The role of the kinesin motor KIF1C in hereditary spastic paraplegia
Challenges and Controversies in the Genetic Diagnosis of Hereditary Spastic Paraplegia
Translational research approaches in hereditary spastic paraplegia
Early-onset hereditary spastic paraplegia: case report
Neurometabolic Dysfunction in SPG11 Hereditary Spastic Paraplegia
Understanding disease modulators of SPG11‐linked hereditary spastic paraplegia.
Neuroinflammatory disease signatures in SPG11-related hereditary spastic paraplegia patients
The role of inflammation in hereditary spastic paraplegia type 11
Hereditary spastic paraplegia from 1880 to 2017: an historical review
Non-pharmacological treatment of hereditary spastic paraplegia: a systematic review
Functional characterization of hereditary spastic paraplegia proteins spastin and ZFYVE27
Gene identification in Hereditary Spastic Paraplegias and characterization of Spastic Paraplegia type 58 (SPG58)
The role of the kinesin motor KIF1C in hereditary spastic paraplegia