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- W2029388085 abstract "The molecular pathogenesis of benign childhood epilepsy with centrotemporal spikes (BECTS) remains unclear whereas mutations of the KCNQ2 and KCNQ3 genes have been identified as causes of benign familial neonatal convulsions. We report here a girl with benign neonatal convulsions followed by BECTS, for whom a mutation of KCNQ2 was identified. This case may provide the clue to the understanding of the molecular pathogenesis of BECTS." @default.
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- W2029388085 date "2012-11-01" @default.
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- W2029388085 title "KCNQ2 abnormality in BECTS: Benign childhood epilepsy with centrotemporal spikes following benign neonatal seizures resulting from a mutation of KCNQ2" @default.
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- W2029388085 doi "https://doi.org/10.1016/j.eplepsyres.2012.07.011" @default.
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