# autosomal recessive spinocerebellar ataxia 14

> Human disease

**Wikidata**: [Q21124567](https://www.wikidata.org/wiki/Q21124567)  
**Source**: https://4ort.xyz/entity/autosomal-recessive-spinocerebellar-ataxia-14


## References

1. Monarch Disease Ontology release 2018-06-29
2. Disease Ontology
3. UniProt
4. Recessive mutations in SPTBN2 implicate β-III spectrin in both cognitive and motor development
5. [Open Targets Platform](https://platform.opentargets.org/evidence/ENSG00000173898/Orphanet_352403)
6. [Identifiers.org](http://www.ebi.ac.uk/miriam/main/collections/MIR:00000233)
7. UMLS 2023