Gene identification in Hereditary Spastic Paraplegias and characterization of Spastic Paraplegia type 58 (SPG58)
- Location
-
Deutsche Nationalbibliothek Frankfurt am Main
- Extent
-
Online-Ressource
- Language
-
Englisch
- Notes
-
Tübingen, Universität Tübingen, Dissertation, 2016
- Keyword
-
Identification
Degeneration
Kinesin
Paraplegia
Genes
Degeneration ; Wissenschaft ; Querschnittslähmung ; Gehirn ; Nervenzelle ; Kinesin ; RNS
- Event
-
Veröffentlichung
- (where)
-
Tübingen
- (who)
-
Universitätsbibliothek Tübingen
- (when)
-
2016
- Creator
-
Oteyza, Andrés de
- Contributor
-
Schöls, Ludger
- URN
-
urn:nbn:de:bsz:21-dspace-731751
- Rights
-
Der Zugriff auf das Objekt ist unbeschränkt möglich.
- Last update
-
15.08.2025, 7:29 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
- Oteyza, Andrés de
- Schöls, Ludger
- Universitätsbibliothek Tübingen
Time of origin
- 2016
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Functional characterization of wild-type and N471D strumpellin in hereditary spastic paraplegia
Generation and characterization of a mouse model for hereditary spastic paraplegia SPG15
Generation and characterization of a murine model for Hereditary Spastic Paraplegia SPG11
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The role of inflammation in hereditary spastic paraplegia type 11
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Functional characterization of wild-type and N471D strumpellin in hereditary spastic paraplegia
Generation and characterization of a mouse model for hereditary spastic paraplegia SPG15
Generation and characterization of a murine model for Hereditary Spastic Paraplegia SPG11
Neuroinflammatory disease signatures in SPG11-related hereditary spastic paraplegia patients
The role of inflammation in hereditary spastic paraplegia type 11
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