Copy number variants--an unexpected risk factor for the idiopathic generalized epilepsies.

Please use this identifier to cite or link to this item: https://ahro.austin.org.au/austinjspui/handle/1/10946

Full metadata record

DC Field	Value	Language
dc.contributor.author	Scheffer, Ingrid E	en
dc.contributor.author	Berkovic, Samuel F	en
dc.date.accessioned	2015-05-16T00:31:26Z
dc.date.available	2015-05-16T00:31:26Z
dc.date.issued	2010-01-01	en
dc.identifier.citation	Brain : A Journal of Neurology; 133(Pt 1): 7-8	en
dc.identifier.govdoc	20047903	en
dc.identifier.other	PUBMED	en
dc.identifier.uri	https://ahro.austin.org.au/austinjspui/handle/1/10946	en
dc.language.iso	en	en
dc.subject.other	DNA Copy Number Variations.genetics	en
dc.subject.other	Epilepsy, Generalized.genetics.physiopathology	en
dc.subject.other	Genetic Variation.genetics	en
dc.subject.other	Humans	en
dc.subject.other	Risk Factors	en
dc.title	Copy number variants--an unexpected risk factor for the idiopathic generalized epilepsies.	en
dc.type	Journal Article	en
dc.identifier.journaltitle	Brain	en
dc.identifier.affiliation	Epilepsy Research Centre, The University of Melbourne, Austin Health, Heidelberg, Victoria Australia	en
dc.identifier.doi	10.1093/brain/awp332	en
dc.description.pages	7-8	en
dc.relation.url	https://pubmed.ncbi.nlm.nih.gov/20047903	en
dc.type.austin	Journal Article	en
local.name.researcher	Berkovic, Samuel F
item.languageiso639-1	en	-
item.openairetype	Journal Article	-
item.openairecristype	http://purl.org/coar/resource_type/c_18cf	-
item.fulltext	With Fulltext	-
item.grantfulltext	open	-
item.cerifentitytype	Publications	-
crisitem.author.dept	Epilepsy Research Centre	-
crisitem.author.dept	Epilepsy Research Centre	-
crisitem.author.dept	Neurology	-
Appears in Collections:	Journal articles

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