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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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| Publicado no: | J Mol Med (Berl) |
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| Main Authors: | , , , , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Springer Berlin Heidelberg
2020
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7524861/ https://ncbi.nlm.nih.gov/pubmed/32851462 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1007/s00109-020-01967-y |
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