| Species | Homo sapiens |
| Epilepsy-Associated Disorder(s) | leptomeningeal glioneuronal heterotopia (cortical dysplasia) |
| Description | empty spiracles homolog 2 |
| Chromosome | 10 |
| Locus | 10q26.1 |
| Reference(s) |
Granata T, Battaglia G, D'Incerti L, Franceschetti S, Spreafico R, Battino D, Savoiardo M, Avanzini G. Schizencephaly: neuroradiologic and epileptologic findings. Epilepsia. 1996 Dec;37(12):1185-93.
Guerrini R, Carrozzo R. Epileptogenic brain malformations: clinical presentation, malformative patterns and indications for genetic testing. Seizure. 2002 Apr;11 Suppl A:532-43; quiz 544-7. Ligon KL, Echelard Y, Assimacopoulos S, Danielian PS, Kaing S, Grove EA, McMahon AP, Rowitch DH. Loss of Emx2 function leads to ectopic expression of Wnt1 in the developing telencephalon and cortical dysplasia. Development. 2003 May;130(10):2275-87. |