Please use this identifier to cite or link to this item: https://ahro.austin.org.au/austinjspui/handle/1/9150
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dc.contributor.authorBerkovic, Samuel Fen
dc.contributor.authorScheffer, Ingriden
dc.date.accessioned2015-05-15T22:07:42Z-
dc.date.available2015-05-15T22:07:42Z-
dc.date.issued1999-04-01en
dc.identifier.citationCurrent Opinion in Neurology; 12(2): 177-82en
dc.identifier.govdoc10226750en
dc.identifier.otherPUBMEDen
dc.identifier.urihttps://ahro.austin.org.au/austinjspui/handle/1/9150en
dc.description.abstractEpilepsies, 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.en
dc.language.isoenen
dc.subject.otherEpilepsy.geneticsen
dc.subject.otherGenetic Linkageen
dc.subject.otherGenetics, Medical.methods.trendsen
dc.subject.otherHumansen
dc.subject.otherIon Channels.geneticsen
dc.subject.otherMolecular Biology.methods.trendsen
dc.subject.otherMutationen
dc.titleGenetics of the epilepsies.en
dc.typeJournal Articleen
dc.identifier.journaltitleCurrent opinion in Neurologyen
dc.identifier.affiliationEpilepsy Research Institute, University of Melbourne, Austin and Repatriation Medical Centre, Australiaen
dc.identifier.doi10.1097/00019052-199904000-00008-
dc.description.pages177-82en
dc.relation.urlhttps://pubmed.ncbi.nlm.nih.gov/10226750en
local.name.researcherBerkovic, Samuel F
item.fulltextNo Fulltext-
item.openairetypeJournal Article-
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
item.grantfulltextnone-
item.languageiso639-1en-
item.cerifentitytypePublications-
crisitem.author.deptEpilepsy Research Centre-
crisitem.author.deptNeurology-
crisitem.author.deptEpilepsy Research Centre-
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