Phenotypes and genotypes in epilepsy with febrile seizures plus
Author:
Publisher
Elsevier BV
Subject
Neurology (clinical),Neurology
Reference19 articles.
1. First genetic evidence of GABAA receptor dysfunction in epilepsy: a mutation in the γ2 subunit gene;Baulac;Nat. Genet.,2001
2. Benign familial neonatal-infantile seizures: characterization of a new sodium channelopathy;Berkovic;Ann. Neurol.,2004
3. De novo mutations in the sodium-channel gene SCN1a cause severe myoclonic epilepsy of infancy;Claes;Am. J. Hum. Genet.,2001
4. Mutations of SCN1A, encoding a neuronal sodium channel, in two families with GEFS+2;Escayg;Nat. Genet.,2000
5. Mutations of sodium channel α sub unit type 1 (SCN1A) in intractable childhood epilepsies with frequent generalized tonic-clonic seizures;Fujiwara;Brain,2003
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