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Striatal Interneurons in Transgenic Nonhuman Primate Model of Huntington’s Disease
Huntington’s disease is an autosomal dominant neurodegenerative disorder associated with progressive motor and cognitive impairments, and the expansion of a cysteine-adenine-guanine trinucleotide (polyglutamine) repeats in exon one of the human huntingtin gene. The pathology of the disease is charac...
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| Publicado no: | Sci Rep |
|---|---|
| Main Authors: | , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Nature Publishing Group UK
2019
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6401084/ https://ncbi.nlm.nih.gov/pubmed/30837611 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1038/s41598-019-40165-w |
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