B Ceulemans

De novo mutations in the sodium-channel gene SCN1A cause severe myoclonic epilepsy of infancy.

L. Lagae, C. Broeckhoven, C. van Broeckhoven, 2001, American journal of human genetics.

Clinical spectrum of early-onset epileptic encephalopathies associated with STXBP1 mutations

I. Scheffer, L. Lagae, S. Berkovic, 2010, Neurology.