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...

ver descrição completa

Na minha lista:
Detalhes bibliográficos
Publicado no:Neuropathol Appl Neurobiol
Main Authors: 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: Artigo
Idioma:Inglês
Publicado em: John Wiley and Sons Inc. 2015
Assuntos:
Original Articles
Acesso em linha: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
Tags: Adicionar Tag
Sem tags, seja o primeiro a adicionar uma tag!

Registos relacionados