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Molecular mechanisms underlying Spinocerebellar Ataxia 17 (SCA17) pathogenesis
Spinocerebellar ataxia 17 (SCA17) belongs to the family of 9 genetically inherited, late-onset neurodegenerative diseases, which are caused by polyglutamine (polyQ) expansion in different proteins. In SCA17, the polyQ expansion occurs in the TATA box binding protein (TBP), which functions as a gener...
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| I publikationen: | Rare Dis |
|---|---|
| Huvudupphovsmän: | , , |
| Materialtyp: | Artigo |
| Språk: | Inglês |
| Publicerad: |
Taylor & Francis
2016
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| Ämnen: | |
| Länkar: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5154381/ https://ncbi.nlm.nih.gov/pubmed/28032013 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1080/21675511.2016.1223580 |
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