Mutations in the GABRA1 and EFHC1 genes are rare in familial juvenile myoclonic epilepsy
Author:
Publisher
Elsevier BV
Subject
Neurology (clinical),Neurology
Reference18 articles.
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2. Commissions on classification and terminology of the International League against epilepsy, 1989. Proposal for revised classification of epilepsies and epileptic syndromes. Epilepsia 30, 389–399.
3. Mutation of GABRA1 in an autosomal dominant form of juvenile myoclonic epilepsy;Cossette;Nat. Genet.,2002
4. Mutations and polymorphisms of the CLCN2 gene in idiopathic epilepsy;D’Agostino;Neurology,2004
5. Juvenile myoclonic epilepsy: characteristics of a primary generalized epilepsy;Dreifuss;Epilepsy,1989
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