Please use this identifier to cite or link to this item: http://ahro.austin.org.au/austinjspui/handle/1/10946
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dc.contributor.authorScheffer, Ingrid Een
dc.contributor.authorBerkovic, Samuel Fen
dc.date.accessioned2015-05-16T00:31:26Z
dc.date.available2015-05-16T00:31:26Z
dc.date.issued2010-01-01en
dc.identifier.citationBrain : A Journal of Neurology; 133(Pt 1): 7-8en
dc.identifier.govdoc20047903en
dc.identifier.otherPUBMEDen
dc.identifier.urihttp://ahro.austin.org.au/austinjspui/handle/1/10946en
dc.language.isoenen
dc.subject.otherDNA Copy Number Variations.geneticsen
dc.subject.otherEpilepsy, Generalized.genetics.physiopathologyen
dc.subject.otherGenetic Variation.geneticsen
dc.subject.otherHumansen
dc.subject.otherRisk Factorsen
dc.titleCopy number variants--an unexpected risk factor for the idiopathic generalized epilepsies.en
dc.typeJournal Articleen
dc.identifier.journaltitleBrainen
dc.identifier.affiliationEpilepsy Research Centre, The University of Melbourne, Austin Health, Heidelberg, Victoria Australiaen
dc.identifier.doi10.1093/brain/awp332en
dc.description.pages7-8en
dc.relation.urlhttp://www.ncbi.nlm.nih.gov/pubmed/20047903en
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