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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Bibliografische gegevens
Gepubliceerd in:Neuropathol Appl Neurobiol
Hoofdauteurs: Lax, Nichola Z., Grady, John, Laude, Alex, Chan, Felix, Hepplewhite, Philippa D., Gorman, Grainne, Whittaker, Roger G., Ng, Yi, Cunningham, Mark O., Turnbull, Doug M.
Formaat: Artigo
Taal:Inglês
Gepubliceerd in: John Wiley and Sons Inc. 2015
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Original Articles
Online toegang: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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