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...

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Detalles Bibliográficos
Autores principales: Sun, Yize, Tong, Huichun, Yang, Tianqi, Liu, Li, Li, Xiao-Jiang, Li, Shihua
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Review
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

Internet

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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