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Ubiquitin-modifying enzymes in Huntington’s disease
Huntington’s disease (HD) is a neurodegenerative disorder caused by a CAG repeat expansion in the N-terminus of the HTT gene. The CAG repeat expansion translates into a polyglutamine expansion in the mutant HTT (mHTT) protein, resulting in intracellular aggregation and neurotoxicity. Lowering the mH...
Autores principales: | Sap, Karen A., Geijtenbeek, Karlijne W., Schipper-Krom, Sabine, Guler, Arzu Tugce, Reits, Eric A. |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10013475/ https://www.ncbi.nlm.nih.gov/pubmed/36926679 http://dx.doi.org/10.3389/fmolb.2023.1107323 |
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