Altered gene transcription profiles in fibroblasts harboring either TK2 or DGUOK mutations indicate compensatory mechanisms

Mitochondrial DNA (mtDNA) depletion syndrome (MDS) is an autosomal recessive disorder characterized by a reduced amount of mtDNA, which impairs synthesis of respiratory chain complexes. MDS has been classified into two main groups, the hepatocerebral form affecting liver and the central nervous syst...

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Detalles Bibliográficos
Publicado en:Exp Cell Res
Main Authors: Villarroya, Joan, de Bolós, Carme, Meseguer, Anna, Hirano, Michio, Vilà, Maya R.
Formato: Artigo
Idioma:Inglês
Publicado: 2009
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Article
Acceso en liña:https://ncbi.nlm.nih.gov/pmc/articles/PMC8285083/
https://ncbi.nlm.nih.gov/pubmed/19265691
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.yexcr.2009.02.018
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