Spinocerebellar Ataxia

Spinocerebellar Ataxia is a rare inherited autosomal dominant disorder that causes progressive cerebellar ataxia. There are different subtypes of the disease underlied by mutations in the Ataxin family of genes, and also calcium ion channel subunit genes.

Axol cell lines derived from Spinocerebellar Ataxia patients and familial and unaffected controls are excellent models for investigating this rare inherited disease.

Axol now offers made-to-order human iPSC-derived brain cells or cardiomyocytes derived from Spinocerebellar Ataxia patients.