Cerebellar contribution to the cognitive alterations in SCA1: evidence from mouse models.
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DOI: 10.1093/hmg/ddz265
Abstract: Spinocerebellar ataxia type 1 (SCA1) is a fatal neurodegenerative disease caused by abnormal expansion of glutamine (Q) encoding CAG repeats in the gene Ataxin-1 (ATXN1). Although motor and balance deficits are the core symptoms of… read more here.
Keywords: alterations sca1; mouse models; cognitive alterations; mice ... See more keywords