Insights into White Matter Defect in Huntington’s Disease

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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Bibliographic Details
Main Authors:	Yize Sun, Huichun Tong, Tianqi Yang, Li Liu, Xiao-Jiang Li, Shihua Li
Format:	Article
Language:	English
Published:	MDPI AG 2022-10-01
Series:	Cells
Subjects:	Huntington’s disease (HD) white matter oligodendrocyte myelin HD animal model
Online Access:	https://www.mdpi.com/2073-4409/11/21/3381

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