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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Autors principals: López, Luis C., Luna-Sánchez, Marta, García-Corzo, Laura, Quinzii, Catarina M., Hirano, Michio
Format: Artigo
Idioma:Inglês
Publicat: S. Karger AG 2014
Matèries:
Published online: March, 2014
Accés en línia: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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