PedAM
Pediatric Disease Annotations & Medicines
| Disease | temporal lobe epilepsy |
| Phenotype | C0149931|migraine |
| Sentences | 2 |
| PubMedID- 21188255 | A linkage analysis in a large belgian family with occipitotemporal lobe epilepsy associated with migraine with visual aura provided evidence for a novel epilepsy and migraine susceptibility locus on chromosome 9q21–q22 (deprez et al., 2007). |
| PubMedID- 20963464 | Moreover, up to 75% of fhm families have a mutation in the p/q-type calcium channel ca(v)2.1 subunit cacna1a gene on chromosome 19p13, while a candidate region of 9.95 cm (5.96 mb) between markers gata152h04 and d9s253 located at chromosome 9q21–q22 was identified in a large belgian family with occipitotemporal lobe epilepsy associated with migraine with visual aura [64]. |
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