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Pathomechanisms in Coenzyme Q(10)-Deficient Human Fibroblasts
Primary coenzyme Q(10) (CoQ(10)) deficiency is a rare mitochondrial disorder associated with 5 major clinical phenotypes: (1) encephalomyopathy, (2) severe infantile multisystemic disease, (3) cerebellar ataxia, (4) isolated myopathy, and (5) steroid-resistant nephrotic syndrome. Growth retardation,...
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| Autores principales: | , , , , |
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| Formato: | Artigo |
| Lenguaje: | Inglês |
| Publicado: |
S. Karger AG
2014
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| Materias: | |
| Acceso en línea: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4112524/ https://ncbi.nlm.nih.gov/pubmed/25126049 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1159/000360494 |
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