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Friedreich Ataxia: Molecular Mechanisms, Redox Considerations, and Therapeutic Opportunities

Mitochondrial dysfunction and oxidative damage are at the origin of numerous neurodegenerative diseases like Friedreich ataxia and Alzheimer and Parkinson diseases. Friedreich ataxia (FRDA) is the most common hereditary ataxia, with one individual affected in 50,000. This disease is characterized by...

Disgrifiad llawn

Wedi'i Gadw mewn:
Manylion Llyfryddiaeth
Prif Awduron: Santos, Renata, Lefevre, Sophie, Sliwa, Dominika, Seguin, Alexandra, Camadro, Jean-Michel, Lesuisse, Emmanuel
Fformat: Artigo
Iaith:Inglês
Cyhoeddwyd: Mary Ann Liebert, Inc. 2010
Pynciau:
Mynediad Ar-lein:https://ncbi.nlm.nih.gov/pmc/articles/PMC2924788/
https://ncbi.nlm.nih.gov/pubmed/20156111
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1089/ars.2009.3015
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