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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Detalles Bibliográficos
Autores principales: 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.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2015
Materias:
Original Articles
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4772453/
https://www.ncbi.nlm.nih.gov/pubmed/25786813
http://dx.doi.org/10.1111/nan.12238

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4772453/
https://www.ncbi.nlm.nih.gov/pubmed/25786813
http://dx.doi.org/10.1111/nan.12238

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