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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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| Publicado no: | J Neuropathol Exp Neurol |
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| Main Authors: | , , , , , , , , , , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Oxford University Press
2016
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| Assuntos: | |
| Acesso em linha: | 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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