Genetic deletion of S6k1 does not rescue the phenotypic deficits observed in the R6/2 mouse model of Huntington’s disease
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DOI: 10.1038/s41598-019-52391-3
Abstract: Huntington’s disease (HD) is a fatal inherited autosomal dominant neurodegenerative disorder caused by an expansion in the number of CAG trinucleotide repeats in the huntingtin gene. The disease is characterized by motor, behavioural and cognitive… read more here.
Keywords: huntington disease; disease; s6k1; s6k1 knockout ... See more keywords