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GENATLAS PHENOTYPE |
last update : 28-06-2017 |
Symbol | FFEVF3 |
Location | 16p13.3 |
Name | familial focal epilepsy with variable foci, 3 |
Corresponding gene | NPRL3 |
Main clinical features |
|
Genetic determination | autosomal dominant |
Function/system disorder | neurology |
Type | disease |
Remark(s) |