Article ID Journal Published Year Pages File Type
9988921 European Journal of Paediatric Neurology 2005 8 Pages PDF
Abstract
This disease is caused by various mutations of genes coding for subunits of neuronal acetylcholine receptor comprising the sodium/potassium ion channel. Recent advances in molecular genetics have provided the means for a better understanding of human epileptogenesis at a molecular level, which can facilitate clinical diagnosis and provides a more rational basis of therapy of this form of epilepsy. In this review, we report the recent data in the genetics of ADNFLE.
Related Topics
Life Sciences Neuroscience Developmental Neuroscience
Authors
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