Human neuronal coenzyme Q10 deficiency results in global loss of mitochondrial respiratory chain activity, increased mitochondrial oxidative stress and reversal of ATP synthase activity: implications for pathogenesis and treatment-Reference-Cited by-同舟云学术

Human neuronal coenzyme Q10 deficiency results in global loss of mitochondrial respiratory chain activity, increased mitochondrial oxidative stress and reversal of ATP synthase activity: implications for pathogenesis and treatment

Published:2012-07-06 Issue:1 Volume:36 Page:63-73
ISSN:0141-8955
Container-title:Journal of Inherited Metabolic Disease
language:en
Short-container-title:J Inherit Metab Dis

Author:

Duberley Kate E. C.,Abramov Andrey Y.,Chalasani Annapurna,Heales Simon J.,Rahman Shamima,Hargreaves Iain P.

Publisher

Wiley

Subject

Genetics (clinical),Genetics

Link

http://www.springerlink.com/index/pdf/10.1007/s10545-012-9511-0

Reference40 articles.

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3. Auré K et al (2004) Progression despite replacement of a myopathic form of coenzyme Progression despite replacement of a myopathic form of coenzyme Q10 defect. Neurology 63(4):727–729

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