Mutant GABAA receptor γ2-subunit in childhood absence epilepsy and febrile seizures

By R. Wallace, C. Marini, S. Petrou, L. Harkin, D. Bowser, R. Panchal, D. Williams, G. Sutherland, J. Mulley, I. Scheffer and 1 more. Nature Genetics, 2001

721 citations recorded by the source corpus.

Subfields: Cellular and Molecular Neuroscience, Molecular Biology, Psychiatry and Mental health

View Paper: https://www.semanticscholar.org/paper/6b512be8f7c27be2936279a1cbc1174739a1d89c

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1. N. Leresche
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Citations in the corpus

• Childhood absence epilepsy: Genes, channels, neurons and networks (2002, background): “In addition, as the arginine→glutamine polymorphism was absent in other CAE (and FS) sufferers that were not included in their study, Wallace et al.22 suggest that this gene mutation “is not a common cause of these syndromes”.”