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Therapeutic Advances for Huntington’s Disease
Huntington’s disease (HD) is a progressive neurological disease that is inherited in an autosomal fashion. The cause of disease pathology is an expansion of cytosine-adenine-guanine (CAG) repeats within the huntingtin gene (HTT) on chromosome 4 (4p16.3), which codes the huntingtin protein (mHTT). Th...
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| Publicado en: | Brain Sci |
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| Main Authors: | , , , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado: |
MDPI
2020
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| Assuntos: | |
| Acceso en liña: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7016861/ https://ncbi.nlm.nih.gov/pubmed/31940909 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3390/brainsci10010043 |
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