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Biomarkers for Detecting Mitochondrial Disorders
(1) Objectives: Mitochondrial disorders (MIDs) are a genetically and phenotypically heterogeneous group of slowly or rapidly progressive disorders with onset from birth to senescence. Because of their variegated clinical presentation, MIDs are difficult to diagnose and are frequently missed in their...
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| Pubblicato in: | J Clin Med |
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| Autori principali: | , |
| Natura: | Artigo |
| Lingua: | Inglês |
| Pubblicazione: |
MDPI
2018
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| Soggetti: | |
| Accesso online: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5852432/ https://ncbi.nlm.nih.gov/pubmed/29385732 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3390/jcm7020016 |
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