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Mitochondrial Structural and Functional Dynamics in Huntington’s Disease

Huntington’s disease (HD) is an autosomal, dominantly inherited neurodegenerative disorder, characterized by chorea, involuntary movements, and cognitive impairments. Tremendous progress has made since the discovery of HD gene in 1993, in terms of developing animal models to study the disease proces...

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Detalhes bibliográficos
Main Authors: Reddy, P. Hemachandra, Mao, Peizhong, Manczak, Maria
Formato: Artigo
Idioma:Inglês
Publicado em: 2009
Assuntos:
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC2748129/
https://ncbi.nlm.nih.gov/pubmed/19394359
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.brainresrev.2009.04.001
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