Autosomal recessive spinocerebellar ataxia 16

Any autosomal recessive cerebellar ataxia in which the cause of the disease is a mutation in the STUB1 gene.

Also known as: SCAR16, STUB1 autosomal recessive cerebellar ataxia, autosomal recessive cerebellar ataxia caused by mutation in STUB1, autosomal recessive spinocerebellar ataxia 16, autosomal recessive spinocerebellar ataxia type 16, spinocerebellar ataxia autosomal recessive type 16, spinocerebellar ataxia, autosomal recessive type 16, autosomal recessive cerebellar ataxia due to STUB1 deficiency

18 clinical trials for this condition and its sub-types, 0 tagged with Autosomal recessive spinocerebellar ataxia 16 itself.