Disease-associated oligodendrocyte signatures are spatiotemporally dysregulated in spinocerebellar ataxia type 3
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DOI: 10.3389/fnins.2023.1118429
Abstract: Spinocerebellar ataxia type 3 (SCA3) is a neurodegenerative disease caused by a CAG repeat expansion in the ATXN3 gene. Though the ATXN3 protein is expressed ubiquitously throughout the CNS, regional pathology in SCA3 patients is… read more here.
Keywords: oligodendrocyte signatures; disease; associated oligodendrocyte; spinocerebellar ataxia ... See more keywords