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The insulin-like growth factor pathway is altered in spinocerebellar ataxia type 1 and type 7
Polyglutamine diseases are inherited neurodegenerative disorders caused by expansion of CAG repeats encoding a glutamine tract in the disease-causing proteins. There are nine disorders, each having distinct features but also clinical and pathological similarities. In particular, spinocerebellar atax...
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| Autors principals: | , , , , , , , , |
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| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
National Academy of Sciences
2008
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| Matèries: | |
| Accés en línia: | https://ncbi.nlm.nih.gov/pmc/articles/PMC2234131/ https://ncbi.nlm.nih.gov/pubmed/18216249 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1073/pnas.0711257105 |
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