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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...
Αποθηκεύτηκε σε:
| Τόπος έκδοσης: | Neuropathol Appl Neurobiol |
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| Κύριοι συγγραφείς: | , , , , , , , , , |
| Μορφή: | Artigo |
| Γλώσσα: | Inglês |
| Έκδοση: |
John Wiley and Sons Inc.
2015
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| Θέματα: | |
| Διαθέσιμο 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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