Mendoza-Ferreira et al., 2018
- Biallelic CHP1 mutation causes human autosomal recessive ataxia by impairing NHE1 function.
Neurology. Genetics
4:e209
Full text @ Neurol Genet
| Human Disease | Fish | Environment | Evidence Code |
|---|---|---|---|
| autosomal recessive cerebellar ataxia |