PedAM
Pediatric Disease Annotations & Medicines
| Disease | ataxia |
| Phenotype | C0154723|migraine with aura |
| Sentences | 1 |
| PubMedID- 22527033 | We report a 54-year-old woman, among the population of the lombardia gens project (http://www.clinicaltrial.gov), affected by migraine with aura and ataxia carrying the p.arg583gln missense substitution in the cacna1a gene focusing, through a review literature, on the clinical phenotype of mutation carriers. |
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