Wordt geladen...
Role of Mitochondrial Dysfunction in the Pathogenesis of Huntington’s Disease
Huntington’s disease (HD) is an autosomal dominant neurodegenerative disorder that is caused by a pathological expansion of CAG repeats within the gene encoding for a 350 kD protein called huntingtin. This polyglutamine expansion within huntingtin is the causative factor in the pathogenesis of HD, h...
Bewaard in:
| Hoofdauteurs: | , |
|---|---|
| Formaat: | Artigo |
| Taal: | Inglês |
| Gepubliceerd in: |
2009
|
| Onderwerpen: | |
| Online toegang: | https://ncbi.nlm.nih.gov/pmc/articles/PMC2757461/ https://ncbi.nlm.nih.gov/pubmed/19622387 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.brainresbull.2009.07.010 |
| Tags: |
Voeg label toe
Geen labels, Wees de eerste die dit record labelt!
|