Genetic knock-down of HDAC3 does not modify disease-related phenotypes in a mouse model of Huntington's disease.

Huntington's disease (HD) is an autosomal dominant progressive neurodegenerative disorder caused by an expansion of a CAG/polyglutamine repeat for which there are no disease modifying treatments. In recent years, transcriptional dysregulation has emerged as a pathogenic process that appears ear...

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Bibliographic Details
Main Authors: Lara Moumné, Ken Campbell, David Howland, Yingbin Ouyang, Gillian P Bates
Format: article
Language:EN
Published: Public Library of Science (PLoS) 2012
Subjects:
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Online Access:https://doaj.org/article/df609b2a2ad04b188d9cdff1e7b1b680
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