PedAM
Pediatric Disease Annotations & Medicines
| Disease | tic disorder |
| Phenotype | C0003635|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. |
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