Please use this identifier to cite or link to this item: https://ahro.austin.org.au/austinjspui/handle/1/20883
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dc.contributor.authorMuir, Alison M-
dc.contributor.authorKing, Chontelle-
dc.contributor.authorSchneider, Amy L-
dc.contributor.authorButtar, Aman S-
dc.contributor.authorScheffer, Ingrid E-
dc.contributor.authorSadleir, Lynette G-
dc.contributor.authorMefford, Heather C-
dc.date2019-06-
dc.date.accessioned2019-06-05T01:28:45Z-
dc.date.available2019-06-05T01:28:45Z-
dc.date.issued2019-06-
dc.identifier.citationNeurology: Genetics 2019; 5(3): e333-
dc.identifier.issn2376-7839-
dc.identifier.urihttps://ahro.austin.org.au/austinjspui/handle/1/20883-
dc.language.isoeng-
dc.titleDouble somatic mosaicism in a child with Dravet syndrome.-
dc.typeJournal Article-
dc.identifier.journaltitleNeurology. Genetics-
dc.identifier.affiliationDepartment of Neurology, Royal Children's Hospital, Parkville, Australiaen
dc.identifier.affiliationEpilepsy Research Centre, Department of Medicine, Austin Health, The University of Melbourne, Heidelberg, Victoria, Australia-
dc.identifier.affiliationDivision of Genetic Medicine, Department of Pediatrics, University of Washington, Seattle, WAen
dc.identifier.affiliationDepartment of Paediatrics and Child Health, University of Otago, Wellington, New Zealanden
dc.identifier.affiliationDepartment of Medicine, The Florey Institute and Murdoch Children's Research Institute, Parkville, Australiaen
dc.identifier.doi10.1212/NXG.0000000000000333-
dc.identifier.orcid0000-0002-2311-2174-
dc.identifier.pubmedid31086826-
dc.type.austinJournal Article-
local.name.researcherScheffer, Ingrid E
item.languageiso639-1en-
item.fulltextNo Fulltext-
item.grantfulltextnone-
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
item.cerifentitytypePublications-
item.openairetypeJournal Article-
crisitem.author.deptEpilepsy Research Centre-
crisitem.author.deptEpilepsy Research Centre-
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