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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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Bibliografische gegevens
Hoofdauteurs: Reddy, P. Hemachandra, Mao, Peizhong, Manczak, Maria
Formaat: Artigo
Taal:Inglês
Gepubliceerd in: 2009
Onderwerpen:
Online toegang: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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