换一批
换一批Regulation of one-carbon metabolism may open new avenues to slow down the initiation and progression of Huntington's disease
摘要Huntington's disease (HD) (OMIM 143100) is an autosomal dominant neurodegenerative disorder caused by a monogenic mutation in the huntingtin gene (HTT), which induces typical midlife onset and age-dependent progression with major symptoms including choreic movements, psychiatric disorders, and cognitive impairment (Gusella et al., 2021).
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