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GENATLAS PHENOTYPE |
last update : 01-07-2015 |
Symbol | ETL7 |
Location | 7q22.1 |
Name | epilepsy, familial temporal lobe, 7 |
Corresponding gene | RELN |
Main clinical features |
|
Genetic determination | autosomal dominant |
Function/system disorder | neurology |
Type | disease |
Remark(s) |