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Lennox-Gastaut Syndrome Press Releases


Severe Childhood Epilepsy Gene Mutations

NIH-funded study discovers new genes for childhood epilepsies
Sunday, Aug 11, 2013
A genetic study of childhood epilepsies has linked two new genes to severe forms of disease and provides a novel strategy for identifying therapy targets. This study used a cutting-edge genetic technique, called exome sequencing, to search for new mutations that are not inherited. The results suggest this may be a highly effective way to find and confirm many disease-causing gene mutations.