Mitochondrial dysfunction and Huntington disease / 神经科学通报·英文版
Neuroscience Bulletin
;
(6): 129-136, 2006.
Article
in English
| WPRIM
| ID: wpr-300946
ABSTRACT
Huntington disease (HD) is a chronic autosomal-dominant neurodegenerative disease. The gene coding Huntingtin has been identified, but the pathogenic mechanisms of the disease are still not fully understood. This paper reviews the involvement of mitochondrial dysfunction in pathogenesis of HD.
Full text:
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Index:
WPRIM (Western Pacific)
Language:
English
Journal:
Neuroscience Bulletin
Year:
2006
Type:
Article
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