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GENETICS AND NEUROPATHOLOGY OF HUNTINGTON’S DISEASE
Huntington’s disease (HD) is an autosomal dominant progressive neurodegenerative disorder that prominently affects the basal ganglia, leading to affective, cognitive, behavioral and motor decline. The basis of HD is a CAG repeat expansion to >35 CAG in a gene that codes for a ubiquitous protein k...
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| 出版年: | Int Rev Neurobiol |
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| 主要な著者: | , , |
| フォーマット: | Artigo |
| 言語: | Inglês |
| 出版事項: |
2011
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| 主題: | |
| オンライン･アクセス: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4458347/ https://ncbi.nlm.nih.gov/pubmed/21907094 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/B978-0-12-381328-2.00014-6 |
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