PedAM
Pediatric Disease Annotations & Medicines
| Disease | epilepsy |
| Phenotype | C1720189|episodic ataxia |
| Sentences | 1 |
| PubMedID- 20156848 | In addition, some patients with episodic ataxia complicated by epilepsy have been shown to harbour cacna1a mutations, raising the possibility that p/q channel dysfunction may be linked to human epilepsy. |
Page: 1