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Expanding and validating the biomarkers for mitochondrial diseases

ABSTRACT: Mitochondrial diseases are highly heterogeneous metabolic disorders caused by genetic alterations in the mitochondrial DNA (mtDNA) or in the nuclear genome. In this study, we investigated a panel of blood biomarkers in a cohort of 123 mitochondrial patients, with prominent neurological and...

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Detalles Bibliográficos
Autores principales:	Maresca, Alessandra, Del Dotto, Valentina, Romagnoli, Martina, La Morgia, Chiara, Di Vito, Lidia, Capristo, Mariantonietta, Valentino, Maria Lucia, Carelli, Valerio
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	Springer Berlin Heidelberg 2020
Materias:	Original Article
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7524861/ https://www.ncbi.nlm.nih.gov/pubmed/32851462 http://dx.doi.org/10.1007/s00109-020-01967-y

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