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Insights into White Matter Defect in Huntington’s Disease
Huntington’s disease (HD) is an autosomal-dominant inherited progressive neurodegenerative disorder. It is caused by a CAG repeat expansion in the Huntingtin gene that is translated to an expanded polyglutamine (PolyQ) repeat in huntingtin protein. HD is characterized by mood swings, involuntary mov...
Autores principales: | Sun, Yize, Tong, Huichun, Yang, Tianqi, Liu, Li, Li, Xiao-Jiang, Li, Shihua |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9656068/ https://www.ncbi.nlm.nih.gov/pubmed/36359783 http://dx.doi.org/10.3390/cells11213381 |
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