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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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| Publicat a: | Front Cell Neurosci |
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| Autors principals: | , , |
| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
Frontiers Media S.A.
2021
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| Matèries: | |
| Accés en línia: | 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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