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Showing articles 0 to 2 of 2 Filter Applied: seizure,familial (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 Neurological Findings in Patients with the Fragile-X Syndrome JNNP 48:150-153, Finelli,P.F.,et al, 1985 Showing articles 0 to 2 of 2