Mitochondria and Parkinson’s Disease: Clinical, Molecular, and Translational Aspects

Mitochondrial dysfunction represents a well-established player in the pathogenesis of both monogenic and idiopathic Parkinson’s disease (PD). Initially originating from the observation that mitochondrial toxins cause PD, findings from genetic PD supported a contribution of mitochondrial dysfunction...

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Detalles Bibliográficos
Autores principales: Borsche, Max, Pereira, Sandro L., Klein, Christine, Grünewald, Anne
Formato: Online Artículo Texto
Lenguaje:English
Publicado: IOS Press 2021
Materias:
Review
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7990451/
https://www.ncbi.nlm.nih.gov/pubmed/33074190
http://dx.doi.org/10.3233/JPD-201981

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7990451/
https://www.ncbi.nlm.nih.gov/pubmed/33074190
http://dx.doi.org/10.3233/JPD-201981

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