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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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Podrobná bibliografie
Hlavní autoři: Reddy, P. Hemachandra, Mao, Peizhong, Manczak, Maria
Médium: Artigo
Jazyk:Inglês
Vydáno: 2009
Témata:
On-line přístup: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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