Modulation of Molecular Chaperones in Huntington's Disease and Other Polyglutamine Disorders
Polyglutamine expansion mutations in specific proteins underlie the pathogenesis of a group of progressive neurodegenerative disorders, including Huntington's disease, spinal and bulbar muscular atrophy, dentatorubral-pallidoluysian atrophy, and several spinocerebellar ataxias. The different mu...
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| Outros Autores: | , |
| Formato: | other |
| Idioma: | eng |
| Publicado em: |
2017
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| Assuntos: | |
| Texto completo: | https://hdl.handle.net/10216/104701 |
| País: | Portugal |
| Oai: | oai:repositorio-aberto.up.pt:10216/104701 |