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GENATLAS PHENOTYPE

last update : 04-02-2014

Symbol	ECA2
Location	5q34
Name	epilepsy, childhood absence 2
Corresponding gene	GABRG2
Other symbol(s)	CAE2
Main clinical features	both childhood absence epilepsy and febrile seizures
Genetic determination	autosomal dominant
Function/system disorder	neurology
Type	susceptibility factor

Gene product

Name	gamma-aminobutyric acid A receptor, gamma 2

Remark(s)