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Therapies for mitochondrial diseases and current clinical trials
Mitochondrial diseases are a clinically and genetically heterogeneous group of disorders that result from dysfunction of the mitochondrial oxidative phosphorylation due to molecular defects in genes encoding mitochondrial proteins. Despite the advances in molecular and biochemical methodologies lead...
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| Pubblicato in: | Mol Genet Metab |
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| Autori principali: | , , , |
| Natura: | Artigo |
| Lingua: | Inglês |
| Pubblicazione: |
2017
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| Soggetti: | |
| Accesso online: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5773113/ https://ncbi.nlm.nih.gov/pubmed/28943110 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.ymgme.2017.09.009 |
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