Spinocerebellar ataxia, autosomal recessive 24

MONDO:0014934

Any autosomal recessive cerebellar ataxia in which the cause of the disease is a mutation in the UBA5 gene.

Also known as: SCAR24, UBA5 autosomal recessive cerebellar ataxia, autosomal recessive cerebellar ataxia caused by mutation in UBA5, spinocerebellar ataxia, autosomal recessive 24, spinocerebellar ataxia, autosomal recessive 24; SCAR24, spinocerebellar ataxia, autosomal recessive type 24

18 clinical trials for this condition and its sub-types, 0 tagged with Spinocerebellar ataxia, autosomal recessive 24 itself.

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↑ Autosomal recessive cerebellar ataxia (72)

Including sub-types (18) Tagged with Spinocerebellar ataxia, autosomal recessive 24 (0)

We haven't found any trials for this condition yet. Follow it to get notified when new trials appear.