Converging Role for REEP1/SPG31 in Oxidative Stress

Mutations in the receptor expression-enhancing protein 1 gene (REEP1) are associated with hereditary spastic paraplegia type 31 (SPG31), a neurological disorder characterized by length-dependent degeneration of upper motor neuron axons. Mitochondrial dysfunctions have been observed in patients harbo...

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Detalles Bibliográficos
Autores principales: Naef, Valentina, Meschini, Maria C., Tessa, Alessandra, Morani, Federica, Corsinovi, Debora, Ogi, Asahi, Marchese, Maria, Ori, Michela, Santorelli, Filippo M., Doccini, Stefano
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2023
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9959426/
https://www.ncbi.nlm.nih.gov/pubmed/36834939
http://dx.doi.org/10.3390/ijms24043527

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9959426/
https://www.ncbi.nlm.nih.gov/pubmed/36834939
http://dx.doi.org/10.3390/ijms24043527

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