PedAM
Pediatric Disease Annotations & Medicines
| Disease | tic disorder |
| Phenotype | C0271270|oculomotor apraxia |
| Sentences | 1 |
| PubMedID- 23593030 | Senataxin, mutated in the human genetic disorder ataxia with oculomotor apraxia type 2 (aoa2), plays an important role in maintaining genome integrity by coordination of transcription, dna replication, and the dna damage response. |
Page: 1