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Clinical Correlations of Mutations in the SCN1A Gene: From Febrile Seizures to Severe Myoclonic Epilepsy in Infancy Pediatr Neurol 30:236-243, Ceulemans,B.P.G.M.,et al, 2004 See this aricle in Pubmed Article Abstract No abstract available for this article

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(click to filter results - removes previous filter) Dravet syndrome familial gene mutation myoclonus,epilepsy SCN1A gene seizure,children seizure,familial seizure,febrile seizure,neonatal

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