Pathogenic variants in the KCNT1 gene, which encodes potassium channel subfamily T member 1, cause a severe childhood developmental epileptic encephalopathy.

In a significant ruling, the High Court awarded Rs 8.9 lakh compensation to the family of a mason who died following a ...

LOS ANGELES -- Low racial diversity has limited genome-wide association studies (GWAS) in epilepsy, researchers found, with ...