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

Internet

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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