# spinocerebellar ataxia type 42

> human disease

**Wikidata**: [Q55345906](https://www.wikidata.org/wiki/Q55345906)  
**Source**: https://4ort.xyz/entity/spinocerebellar-ataxia-type-42


## References

1. Monarch Disease Ontology release 2018-06-29
2. Disease Ontology
3. UniProt
4. A Recurrent Mutation in CACNA1G Alters Cav3.1 T-Type Calcium-Channel Conduction and Causes Autosomal-Dominant Cerebellar Ataxia
5. [Open Targets Platform](https://platform.opentargets.org/evidence/ENSG00000006283/EFO_0009059)
6. [Identifiers.org](https://registry.identifiers.org/registry/doid)