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|Title:||Genetics of the epilepsies.||Austin Authors:||Berkovic, Samuel F ;Scheffer, Ingrid||Affiliation:||Epilepsy Research Institute, University of Melbourne, Austin and Repatriation Medical Centre, Australia||Issue Date:||1-Apr-1999||Publication information:||Current Opinion in Neurology; 12(2): 177-82||Abstract:||Epilepsies, like other common diseases, have complex inheritance, and molecular genetic studies in such conditions are difficult. There has been recent success in identifying the molecular basis of certain epilepsies, particularly in those syndromes with autosomal dominant inheritance. All four genes discovered to date for idiopathic epilepsies code for ion channel subunits, either ligand-gated or voltage-gated. The idiopathic epilepsies thus appear, at least in part, to be a family of channelopathies.||Gov't Doc #:||10226750||URI:||http://ahro.austin.org.au/austinjspui/handle/1/9150||DOI:||10.1097/00019052-199904000-00008||URL:||https://pubmed.ncbi.nlm.nih.gov/10226750||Type:||Journal Article||Subjects:||Epilepsy.genetics
|Appears in Collections:||Journal articles|
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