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A Locus for Febrile Seizures (FEB3) Maps to Chromosome 2q23-24
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Genetic Localization of the Familial Adult Myoclonic Epilepsy (FAME) Gene to Chromosome 8q24
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X-Linked Malformation of Neuronal Migration
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Periventricular Heterotopia and Epilepsy
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Reduced GABA Synthesis in Pyridoxine-Dependent Seizures
Lancet 343:1133-1134, Gospe,S.M.,et al, 1994
Seizure Characteristics in Chromosome 20 Benign Familial Neonatal Convulsions
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Juvenile Myoclonic Epilepsy, Underdiagnosed and Treatment May Have to be Life Long
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Delayed Diagnosis of Juvenile Myoclonic Epilepsy
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Benign Familial Neonatal Convulsions:Evidence for Clinical and Genetic Heterogeneity
Ann Neurol 29:469-473, Ryan,S.G.,et al, 1991
Localization of Idiopathic Generalized Epilepsy on Chromosome 6p in Families of Juvenile Myoclonic epilepsy patients
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Monozygotic Twins with Seizures, Shared Characteristics
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Hereditary Long Q-T Syndrome Presenting as Epilepsy:Electroencephalography Laboratory Diagnosis
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Juvenile Myoclonic Epilepsy:An Autosomal Recessive Disease
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