Loading...

Mitochondrial alterations accompanied by oxidative stress conditions in skin fibroblasts of Huntington’s disease patients

Huntington disease (HD) is an autosomal dominant neurodegenerative disorder manifesting as progressive impairment of motor function and different neuropsychiatric symptoms caused by an expansion of CAG repeats in huntingtin gene (HTT). Mitochondrial dysfunction and bioenergetic defects can contribut...

Fuld beskrivelse

Na minha lista:
Bibliografiske detaljer
Udgivet i:Metab Brain Dis
Main Authors: Jędrak, Paulina, Mozolewski, Paweł, Węgrzyn, Grzegorz, Więckowski, Mariusz R.
Format: Artigo
Sprog:Inglês
Udgivet: Springer US 2018
Fag:
Online adgang:https://ncbi.nlm.nih.gov/pmc/articles/PMC6244791/
https://ncbi.nlm.nih.gov/pubmed/30120672
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1007/s11011-018-0308-1
Tags: Tilføj Tag
Ingen Tags, Vær først til at tagge denne postø!