Association of Mitochondrial Genomic Background with Risk of Multiple System Atrophy

INTRODUCTION: Multiple system atrophy (MSA) is a rare, sporadic, and progressive neurodegenerative disease which is characterised neuropathologically by alpha-synuclein aggregates in oligodendroglia, and clinically by parkinsonism, ataxia, and autonomic dysfunction. Mitochondrial health influences n...

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Publicat a:Parkinsonism Relat Disord
Autors principals: Valentino, Rebecca R., Heckman, Michael G., Johnson, Patrick W., Soto-Beasley, Alexandra I., Walton, Ronald L., Koga, Shunsuke, Uitti, Ryan J., Wszolek, Zbigniew K., Dickson, Dennis W., Ross, Owen A.
Format: Artigo
Idioma:Inglês
Publicat: 2020
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Article
Accés en línia:https://ncbi.nlm.nih.gov/pmc/articles/PMC7769955/
https://ncbi.nlm.nih.gov/pubmed/33189969
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.parkreldis.2020.10.040
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