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Huntingtin and the Synapse
Huntington disease (HD) is a monogenic disease that results in a combination of motor, psychiatric and cognitive symptoms. HD is caused by a CAG trinucleotide repeat expansion in the huntingtin (HTT) gene, which results in the production of a pathogenic mutant HTT protein (mHTT). Although there is n...
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| 出版年: | Front Cell Neurosci |
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| 主要な著者: | , , |
| フォーマット: | Artigo |
| 言語: | Inglês |
| 出版事項: |
Frontiers Media S.A.
2021
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| 主題: | |
| オンライン･アクセス: | https://ncbi.nlm.nih.gov/pmc/articles/PMC8239291/ https://ncbi.nlm.nih.gov/pubmed/34211373 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3389/fncel.2021.689332 |
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