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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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| Vydáno v: | Mol Genet Metab |
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| Hlavní autoři: | , , , |
| Médium: | Artigo |
| Jazyk: | Inglês |
| Vydáno: |
2017
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| Témata: | |
| On-line přístup: | 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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