Making sense of nonsense GABAA receptor mutations associated with genetic epilepsies
Author:
Publisher
Elsevier BV
Subject
Molecular Biology,Molecular Medicine
Reference75 articles.
1. The prevalence and incidence of convulsive disorders in children;Hauser;Epilepsia,1994
2. Human epilepsies: interaction of genetic and acquired factors;Berkovic;Trends Neurosci.,2006
3. Genetics of idiopathic epilepsies;Hirose;Epilepsia,2005
4. Mutant GABAA receptor γ2-subunit in childhood absence epilepsy and febrile seizures;Wallace;Nat. Genet.,2001
5. A mutation in the GABAA receptor α1-subunit is associated with absence epilepsy;Maljevic;Ann. Neurol.,2006
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