Clinical Spectrum of Mutations in SCN1A Gene: Severe Myoclonic Epilepsy in Infancy and Related EpilepsiesEpilepsy Res 70S:S223-S230, Fujiwara,T., 2006
Clinicopath ConfTuberous Sclerosis, Case 41-1986, NEJM 315:1013-1022986., , 1986