Please use this identifier to cite or link to this item: https://ahro.austin.org.au/austinjspui/handle/1/11182
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dc.contributor.authorScheffer, Ingrid Een
dc.date.accessioned2015-05-16T00:46:12Z
dc.date.available2015-05-16T00:46:12Z
dc.date.issued2011-01-01en
dc.identifier.citationEpilepsia; 52(1): 192-3; discussion 193-6en
dc.identifier.govdoc21219310en
dc.identifier.otherPUBMEDen
dc.identifier.urihttps://ahro.austin.org.au/austinjspui/handle/1/11182en
dc.language.isoenen
dc.subject.otherChannelopathies.complications.geneticsen
dc.subject.otherEpilepsy.complications.geneticsen
dc.subject.otherHumansen
dc.subject.otherMutation.geneticsen
dc.subject.otherPhenotypeen
dc.titleGenetics of the epilepsies: channelopathies and beyond.en
dc.typeJournal Articleen
dc.identifier.journaltitleEpilepsiaen
dc.identifier.affiliationThe University of Melbourne Austin Health and Royal Children's Hospital Melbourne, Victoria, Australiaen
dc.identifier.doi10.1111/j.1528-1167.2010.02934.xen
dc.description.pages192-3; discussion 193-6en
dc.relation.urlhttps://pubmed.ncbi.nlm.nih.gov/21219310en
dc.type.austinJournal Articleen
local.name.researcherScheffer, Ingrid E
item.grantfulltextnone-
item.openairetypeJournal Article-
item.languageiso639-1en-
item.fulltextNo Fulltext-
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
item.cerifentitytypePublications-
crisitem.author.deptEpilepsy Research Centre-
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