PedAM
Pediatric Disease Annotations & Medicines
| Disease | cerebellar ataxia |
| Phenotype | C0524851|neurodegenerative disease |
| Sentences | 1 |
| PubMedID- 25327705 | This concept is best illustrated by a catalytic tdp1 mutant that forms the molecular basis of the autosomal recessive neurodegenerative disease spinocerebellar ataxia with axonal neuropathy, and results in an increased stability of its tdp1-dna reaction intermediate. |
Page: 1