Epilepsy, idiopathic generalized, susceptibility to, 13

An inherited susceptibility or predisposition to developing juvenile myclonic epilepsy, idiopathic generalized epilepsy, or childhood absence epilepsy in which the cause of the disease is a mutation in the GABRA1 gene.

Also known as: EIG13, epilepsy, idiopathic generalized, susceptibility to, 13, epilepsy, idiopathic generalized, susceptibility to, type 13, susceptibility to idiopathic generalised epilepsy 13, susceptibility to idiopathic generalized epilepsy 13, GABRA1 juvenile myoclonic epilepsy, epilepsy, childhood absence, susceptibility to, 4, epilepsy, juvenile myoclonic, susceptibility to, 5

0 clinical trials for this condition and its sub-types, 0 tagged with Epilepsy, idiopathic generalized, susceptibility to, 13 itself.