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Spinocerebellar ataxia 48: SCA48, autosomal dominant

Disease ID:1287
Name:Spinocerebellar ataxia 48: SCA48, autosomal dominant
Associated with:1 target
Description
An autosomal dominant neurodegenerative disorder that is characterised by the onset of gait ataxia and/or cognitive-affective symptoms in midadulthood. Caused by heterozygous mutations in the STUB1 gene concurrently with an expanded repeat allele of the TBP gene.
Database Links
OMIM: 618093

Targets

STIP1 homology and U-box containing protein 1

Ligands

No ligand related data available for Spinocerebellar ataxia 48: SCA48, autosomal dominant