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Salvaging hope: Is increasing NAD(+) a key to treating mitochondrial myopathy?
Mitochondrial diseases can arise from mutations either in mitochondrial DNA or in nuclear DNA encoding mitochondrially destined proteins. Currently, there is no cure for these diseases although treatments to ameliorate a subset of the symptoms are being developed. In this issue of EMBO Molecular Med...
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| Autori principali: | , |
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| Natura: | Artigo |
| Lingua: | Inglês |
| Pubblicazione: |
Blackwell Publishing Ltd
2014
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| Soggetti: | |
| Accesso online: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4203349/ https://ncbi.nlm.nih.gov/pubmed/24838280 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.15252/emmm.201404179 |
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