Epilepsy, childhood absence, susceptibility to, 5

Any childhood absence epilepsy in which the cause of the disease is a mutation in the GABRB3 gene.

Also known as: ECA5, childhood absence epilepsy caused by mutation in GABRB3, epilepsy, childhood absence, susceptibility to, 5, epilepsy, childhood absence, susceptibility to, type 5, susceptibility to childhood absence epilepsy 5, GABRB3 childhood absence epilepsy

0 clinical trials for this condition and its sub-types, 0 tagged with Epilepsy, childhood absence, susceptibility to, 5 itself.