PedAM
Pediatric Disease Annotations & Medicines
| Disease | ataxia |
| Phenotype | C0027765|neurologic disorders |
| Sentences | 1 |
| PubMedID- 23077024 | To investigate further the frequency, spectrum, and phenotype of prrt2 mutations, we analyzed this gene in 3 large series of episodic neurologic disorders with pkd/ic, episodic ataxia (ea), and hemiplegic migraine (hm). |
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