SCA3_RNA-Seq Data Access Committee

James D. Mills
j.d.mills@amsterdamumc.nl

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Dataset ID	Description	Technology	Samples
EGAD00001009317	Spinocerebellar ataxia type 3 (SCA3) is the most common autosomal dominant inherited ataxia worldwide, caused by a CAG repeat expansion in the Ataxin-3 gene resulting in a polyglutamine (polyQ)-expansion in the corresponding protein. Here we have RNA-sequencing data from the cerebellum of individuals with SCA3 and matched controls.	Illumina HiSeq 2000	12