Energy metabolism defects in Huntington's disease and effects of coenzyme Q10
Author:
Publisher
Wiley
Subject
Clinical Neurology,Neurology
Reference35 articles.
1. A novel gene containing a trinucleotide repeat that is expanded and unstable on Huntington's disease chromosomes
2. Widespread expression of the human and rat Huntington's disease gene in brain and nonneural tissues
3. Does impairment of energy metabolism result in excitotoxic neuronal death in neurodegenerative illnesses?
4. Alternative excitotoxic hypotheses
5. Huntingtin and DRPLA proteins selectively interact with the enzyme GAPDH
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