PedAM
Pediatric Disease Annotations & Medicines
| Disease | epilepsy |
| Phenotype | C0016667|fragile x syndrome |
| Sentences | 2 |
| PubMedID- 21890420 | Predisposition to epilepsy in fragile x syndrome: does the val66met polymorphism in the bdnf gene play a role. |
| PubMedID- 25857623 | Surgical treatment for medically refractory focal epilepsy in a patient with fragile x syndrome. |
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