Clinical correlations of mutations in the SCN1A gene: from febrile seizures to severe myoclonic epilepsy in infancy

Author:

Ceulemans Berten P.G.M,Claes Lieve R.F,Lagae Lieven G

Publisher

Elsevier BV

Subject

Clinical Neurology,Developmental Neuroscience,Neurology,Pediatrics, Perinatology, and Child Health

Reference36 articles.

1. Les épilepsies graves de l'enfant;Dravet;Vie Méd,1978

2. International League Against Epilepsy (ILAE) Commission Report;Engel;Epilepsia,2001

3. Dravet C, Bureau M, Oguni H, Fukuyama Y, Cokar O. Severe myoclonic epilepsy in infancy (Dravet syndrome). In: Roger J, Bureau M, Dravet C, Genton P, Tassinari CA, Wolf P, editors. Epileptic syndromes in infancy, childhood and adolescence, 3rd ed. Eastleigh, UK: John Libbey & Co. Ltd, 2002:81-103

4. De novo mutations in the sodium-channel gene SCN1A cause severe myoclonic epilepsy of infancy;Claes;Am J Hum Genet,2001

5. Frequent mutations of SCN1A in severe myoclonic epilepsy in infancy;Sugawara;Neurology,2002

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