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The long and the short of aberrant ciliogenesis in Huntington disease
Huntington disease (HD) is a dominantly inherited neurodegenerative disorder that is caused by a mutant huntingtin (HTT) gene encoding a version of the Htt protein with an expanded polyglutamine stretch. Although the HTT gene was discovered more than 18 years ago, the functions of normal Htt and the...
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| Main Authors: | , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
American Society for Clinical Investigation
2011
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| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3204854/ https://ncbi.nlm.nih.gov/pubmed/21985782 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1172/JCI60243 |
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