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Showing articles 0 to 3 of 3 Filter Applied: chromosome 2 (Click to remove) Clinical Spectrum of Mutations in SCN1A Gene: Severe Myoclonic Epilepsy in Infancy and Related Epilepsies Epilepsy Res 70S:S223-S230, Fujiwara,T., 2006 Epilepsy Syndromes in Infancy Pediatr Neurol 34:253-263, Korff,C.M. &Nordii,D.R.,Jr., 2006 A Locus for Febrile Seizures (FEB3) Maps to Chromosome 2q23-24 Ann Neurol 46:671-678, Peiffer,A.,et al, 1999 Showing articles 0 to 3 of 3