Mitochondrial dysfunction and Huntington disease / 神经科学通报·英文版
Neuroscience Bulletin
;
(6): 129-136, 2006.
Artigo
em Inglês
| 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.
Texto completo:
DisponíveL
Índice:
WPRIM (Pacífico Ocidental)
Idioma:
Inglês
Revista:
Neuroscience Bulletin
Ano de publicação:
2006
Tipo de documento:
Artigo
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