PedAM
Pediatric Disease Annotations & Medicines
| Disease | cerebellar ataxia |
| Phenotype | C0042875|vitamin e deficiency |
| Sentences | 1 |
| PubMedID- 22720116 | Furthermore, mutations in the gene coding for the α-tocopherol transporter protein (α-ttp) result in a neurologic syndrome of spinocerebellar ataxia called ataxia with vitamin e deficiency or aved. |
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