PedAM
Pediatric Disease Annotations & Medicines
| Disease | optic atrophy 1 |
| Phenotype | C0524851|neurodegenerative disorders |
| Sentences | 1 |
| PubMedID- 21031019 | Moreover, mutations in mitochondrial proteins (e.g., dynamin-like guanosine triphosphatase [gtpase] optic atrophy 1 [opa1]) are associated with optic neurodegenerative disorders [143]. |
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