The gene coding for PGC-1α modifies age at onset in Huntington's Disease

Huntington's disease (HD) is one of the most common autosomal dominant inherited, neurodegenerative disorders. It is characterized by progressive motor, emotional and cognitive dysfunction. In addition metabolic abnormalities such as wasting and altered energy expenditure are increasingly recog...

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Detalhes bibliográficos
Main Authors: Weydt, Patrick, Soyal, Selma M, Gellera, Cinzia, DiDonato, Stefano, Weidinger, Claus, Oberkofler, Hannes, Landwehrmeyer, G Bernhard, Patsch, Wolfgang
Formato: Artigo
Idioma:Inglês
Publicado em: BioMed Central 2009
Assuntos:
Short Report
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC2630305/
https://ncbi.nlm.nih.gov/pubmed/19133136
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/1750-1326-4-3
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