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Invertebrate Models for Coenzyme Q(10) Deficiency
The human syndrome of coenzyme Q (CoQ) deficiency is a heterogeneous mitochondrial disease characterized by a diminution of CoQ content in cells and tissues that affects all the electron transport processes CoQ is responsible for, like the electron transference in mitochondria for respiration and AT...
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| Autors principals: | , , , |
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| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
S. Karger AG
2014
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| Matèries: | |
| Accés en línia: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4112529/ https://ncbi.nlm.nih.gov/pubmed/25126050 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1159/000362751 |
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