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Extensive respiratory chain defects in inhibitory interneurones in patients with mitochondrial disease
AIMS: Mitochondrial disorders are among the most frequently inherited cause of neurological disease and arise due to mutations in mitochondrial or nuclear DNA. Currently, we do not understand the specific involvement of certain brain regions or selective neuronal vulnerability in mitochondrial disea...
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| Pubblicato in: | Neuropathol Appl Neurobiol |
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| Autori principali: | , , , , , , , , , |
| Natura: | Artigo |
| Lingua: | Inglês |
| Pubblicazione: |
John Wiley and Sons Inc.
2015
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| Soggetti: | |
| Accesso online: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4772453/ https://ncbi.nlm.nih.gov/pubmed/25786813 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1111/nan.12238 |
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