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Metabolomes of mitochondrial diseases and inclusion body myositis patients: treatment targets and biomarkers

Mitochondrial disorders (MDs) are inherited multi‐organ diseases with variable phenotypes. Inclusion body myositis (IBM), a sporadic inflammatory muscle disease, also shows mitochondrial dysfunction. We investigated whether primary and secondary MDs modify metabolism to reveal pathogenic pathways an...

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Detalles Bibliográficos
Autores principales:	Buzkova, Jana, Nikkanen, Joni, Ahola, Sofia, Hakonen, Anna H, Sevastianova, Ksenia, Hovinen, Topi, Yki‐Järvinen, Hannele, Pietiläinen, Kirsi H, Lönnqvist, Tuula, Velagapudi, Vidya, Carroll, Christopher J, Suomalainen, Anu
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	John Wiley and Sons Inc. 2018
Materias:	Research Articles
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6284386/ https://www.ncbi.nlm.nih.gov/pubmed/30373890 http://dx.doi.org/10.15252/emmm.201809091

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