SOD1 in ALS: Taking Stock in Pathogenic Mechanisms and the Role of Glial and Muscle Cells

Amyotrophic lateral sclerosis (ALS) is a fatal neurodegenerative disorder characterized by the loss of motor neurons in the brain and spinal cord. While the exact causes of ALS are still unclear, the discovery that familial cases of ALS are related to mutations in the Cu/Zn superoxide dismutase (SOD...

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Detalles Bibliográficos
Autores principales: Peggion, Caterina, Scalcon, Valeria, Massimino, Maria Lina, Nies, Kelly, Lopreiato, Raffaele, Rigobello, Maria Pia, Bertoli, Alessandro
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Review
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9032988/
https://www.ncbi.nlm.nih.gov/pubmed/35453299
http://dx.doi.org/10.3390/antiox11040614

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9032988/
https://www.ncbi.nlm.nih.gov/pubmed/35453299
http://dx.doi.org/10.3390/antiox11040614

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