Epilepsy, familial focal, with variable foci 2

Any epilepsy, familial focal, with variable foci in which the cause of the disease is a mutation in the NPRL2 gene.

Also known as: FFEVF2, NPRL2 epilepsy, familial focal, with variable foci, epilepsy, familial focal, with variable foci 2, epilepsy, familial focal, with variable foci 2; FFEVF2, epilepsy, familial focal, with variable foci caused by mutation in NPRL2, epilepsy, familial focal, with variable foci type 2

10 clinical trials for this condition and its sub-types.