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Cystathionine γ-lyase deficiency mediates neurodegeneration in Huntington’s disease
Huntington’s disease is an autosomal dominant disease associated with a mutation in the gene encoding huntingtin (Htt) leading to expanded polyglutamine repeats of mutant Htt (mHtt) that elicit oxidative stress, neurotoxicity, and motor and behavioural changes(1). Huntington’s disease is characteriz...
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| 出版年: | Nature |
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| 主要な著者: | , , , , , , |
| フォーマット: | Artigo |
| 言語: | Inglês |
| 出版事項: |
2014
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| 主題: | |
| オンライン･アクセス: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4349202/ https://ncbi.nlm.nih.gov/pubmed/24670645 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1038/nature13136 |
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