Decreased Coenzyme Q10 Levels in Multiple System Atrophy Cerebellum

In familial and sporadic multiple system atrophy (MSA) patients, deficiency of coenzyme Q(10) (CoQ(10)) has been associated with mutations in COQ2, which encodes the second enzyme in the CoQ(10) biosynthetic pathway. Cerebellar ataxia is the most common presentation of CoQ(10) deficiency, suggesting...

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Vydáno v:J Neuropathol Exp Neurol
Hlavní autoři: Barca, Emanuele, Kleiner, Giulio, Tang, Guomei, Ziosi, Marcello, Tadesse, Saba, Masliah, Eliezer, Louis, Elan D., Faust, Phyllis, Kang, Un J, Torres, Jose, Cortes, Etty P., Vonsattel, Jean-Paul G., Kuo, Sheng-Han, Quinzii, Catarina M.
Médium: Artigo
Jazyk:Inglês
Vydáno: Oxford University Press 2016
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Original Articles
On-line přístup:https://ncbi.nlm.nih.gov/pmc/articles/PMC4913434/
https://ncbi.nlm.nih.gov/pubmed/27235405
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/jnen/nlw037
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