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The insulin-like growth factor pathway is altered in spinocerebellar ataxia type 1 and type 7
Polyglutamine diseases are inherited neurodegenerative disorders caused by expansion of CAG repeats encoding a glutamine tract in the disease-causing proteins. There are nine disorders, each having distinct features but also clinical and pathological similarities. In particular, spinocerebellar atax...
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| 主要な著者: | , , , , , , , , |
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| フォーマット: | Artigo |
| 言語: | Inglês |
| 出版事項: |
National Academy of Sciences
2008
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| 主題: | |
| オンライン･アクセス: | https://ncbi.nlm.nih.gov/pmc/articles/PMC2234131/ https://ncbi.nlm.nih.gov/pubmed/18216249 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1073/pnas.0711257105 |
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