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• W2069836023 abstract "Abstract Objective A major goal of epilepsy research is to understand the molecular and functional basis of seizure genesis. A human GABA A γ2 gene mutation (R43Q) is associated with generalized epilepsy. Introduction of this mutation into a mouse by gene targeting recapitulates the human phenotype demonstrating a strong genotype to phenotype link. GABA A receptors play a role in the moment‐to‐moment control of brain function and also on the long‐term wiring of the brain by directing neuronal development. Our objective was to determine whether developmental expression of the mutation alters seizure susceptibility later in life. Methods A tetracycline‐based conditional model for activation of a hypomorphic Q43 disease allele was created and validated. Seizure susceptibility was assessed using the subcutaneous pentylenetetrazole model. Results Seizure susceptibility was significantly reduced in mice where the Q43 allele was suppressed during development. Interpretation These results demonstrate that a human epilepsy‐causing mutation impacts network stability during a critical developmental period. These data suggest that identification of presymptomatic children may provide a window for therapeutic intervention before overt symptoms are observed, potentially altering the course of epileptogenesis. Ann Neurol 2008" @default.
• W2069836023 created "2016-06-24" @default.
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• W2069836023 date "2008-09-28" @default.
• W2069836023 modified "2023-10-18" @default.
• W2069836023 title "Developmental impact of a familial GABA_Areceptor epilepsy mutation" @default.
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• W2069836023 doi "https://doi.org/10.1002/ana.21440" @default.
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