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Quantification of Huntington’s Disease Related Markers in the R6/2 Mouse Model
Huntington’s disease (HD) is caused by an expansion of CAG triplets in the huntingtin gene, leading to severe neuropathological changes that result in a devasting and lethal phenotype. Neurodegeneration in HD begins in the striatum and spreads to other brain regions such as cortex and hippocampus, c...
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| Publicado en: | Front Mol Neurosci |
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| Main Authors: | , , , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado: |
Frontiers Media S.A.
2021
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| Assuntos: | |
| Acceso en liña: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7831778/ https://ncbi.nlm.nih.gov/pubmed/33505246 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3389/fnmol.2020.617229 |
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