Please use this identifier to cite or link to this item: https://ahro.austin.org.au/austinjspui/handle/1/12032
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dc.contributor.authorHildebrand, Michael Sen
dc.contributor.authorDamiano, John Anthonyen
dc.contributor.authorMullen, Saul Aen
dc.contributor.authorBellows, Susannah Ten
dc.contributor.authorScheffer, Ingrid Een
dc.contributor.authorBerkovic, Samuel Fen
dc.date.accessioned2015-05-16T01:40:34Z
dc.date.available2015-05-16T01:40:34Z
dc.date.issued2014-01-10en
dc.identifier.citationHuman Genetics 2014; 133(5): 673-4en
dc.identifier.govdoc24408008en
dc.identifier.otherPUBMEDen
dc.identifier.urihttps://ahro.austin.org.au/austinjspui/handle/1/12032en
dc.language.isoenen
dc.subject.otherDNA Copy Number Variationsen
dc.subject.otherEpilepsy, Absence.geneticsen
dc.subject.otherFemaleen
dc.subject.otherHumansen
dc.subject.otherMaleen
dc.subject.otherMembrane Proteins.geneticsen
dc.titleDoes variation in NIPA2 contribute to genetic generalized epilepsy?en
dc.typeJournal Articleen
dc.identifier.journaltitleHuman geneticsen
dc.identifier.affiliationDepartment of Medicine, Epilepsy Research Centre, University of Melbourne, Austin Health, Heidelberg, VIC, 3084, Australiaen
dc.identifier.doi10.1007/s00439-013-1414-0en
dc.description.pages673-4en
dc.relation.urlhttps://pubmed.ncbi.nlm.nih.gov/24408008en
dc.type.austinJournal Articleen
local.name.researcherBerkovic, Samuel F
item.openairetypeJournal Article-
item.cerifentitytypePublications-
item.fulltextWith Fulltext-
item.grantfulltextopen-
item.languageiso639-1en-
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
crisitem.author.deptEpilepsy Research Centre-
crisitem.author.deptMedicine (University of Melbourne)-
crisitem.author.deptEpilepsy Research Centre-
crisitem.author.deptEpilepsy Research Centre-
crisitem.author.deptEpilepsy Research Centre-
crisitem.author.deptNeurology-
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