Survival transcriptome in the coenzyme Q(10) deficiency syndrome is acquired by epigenetic modifications: a modelling study for human coenzyme Q(10) deficiencies

OBJECTIVES: Coenzyme Q(10) (CoQ(10)) deficiency syndrome is a rare condition that causes mitochondrial dysfunction and includes a variety of clinical presentations as encephalomyopathy, ataxia and renal failure. First, we sought to set up what all have in common, and then investigate why CoQ(10) sup...

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Bibliografski detalji
Glavni autori: Fernández-Ayala, Daniel J M, Guerra, Ignacio, Jiménez-Gancedo, Sandra, Cascajo, Maria V, Gavilán, Angela, DiMauro, Salvatore, Hirano, Michio, Briones, Paz, Artuch, Rafael, De Cabo, Rafael, Salviati, Leonardo, Navas, Plácido
Format: Artigo
Jezik:Inglês
Izdano: BMJ Publishing Group 2013
Teme:
Genetics and Genomics
Online pristup:https://ncbi.nlm.nih.gov/pmc/articles/PMC3612821/
https://ncbi.nlm.nih.gov/pubmed/23533218
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1136/bmjopen-2012-002524
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