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Making (anti-) sense out of huntingtin levels in Huntington disease
BACKGROUND: Huntington disease (HD) is an autosomal dominant neurodegenerative disorder, characterized by motor, psychiatric and cognitive symptoms. HD is caused by a CAG repeat expansion in the first exon of the HTT gene, resulting in an expanded polyglutamine tract at the N-terminus of the hunting...
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| Udgivet i: | Mol Neurodegener |
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| Main Authors: | , , , , , , , |
| Format: | Artigo |
| Sprog: | Inglês |
| Udgivet: |
BioMed Central
2015
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| Fag: | |
| Online adgang: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4411791/ https://ncbi.nlm.nih.gov/pubmed/25928884 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s13024-015-0018-7 |
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