# spinocerebellar ataxia type 28

> Spinocerebellar ataxia type 28 (SCA28) is a very rare subtype of type I autosomal dominant cerebellar ataxia (ADCA type I; see this term). It is characterized by juvenile onset, slowly progressive cerebellar ataxia due to Purkinje cell degeneration.

**Wikidata**: [Q21097868](https://www.wikidata.org/wiki/Q21097868)  
**Source**: https://4ort.xyz/entity/spinocerebellar-ataxia-type-28


## References

1. Monarch Disease Ontology release 2018-06-29
2. Disease Ontology
3. UniProt
4. Mutations in the mitochondrial protease gene AFG3L2 cause dominant hereditary ataxia SCA28
5. [Open Targets Platform](https://platform.opentargets.org/evidence/ENSG00000141385/MONDO_0012450)
6. [Identifiers.org](https://registry.identifiers.org/registry/doid)