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Please use this identifier to cite or link to this item: https://ahro.austin.org.au/austinjspui/handle/1/19403
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dc.contributor.authorMyers, Kenneth A-
dc.contributor.authorWhite, Susan M-
dc.contributor.authorMohammed, Shehla-
dc.contributor.authorMetcalfe, Kay A-
dc.contributor.authorFry, Andrew E-
dc.contributor.authorWraige, Elisabeth-
dc.contributor.authorVasudevan, Pradeep C-
dc.contributor.authorBalasubramanian, Meena-
dc.contributor.authorScheffer, Ingrid E-
dc.date2018-08-10-
dc.date.accessioned2018-09-17T01:47:05Z-
dc.date.available2018-09-17T01:47:05Z-
dc.date.issued2018-08-10-
dc.identifier.citationEpilepsy research 2018; online first: 10 August-
dc.identifier.urihttps://ahro.austin.org.au/austinjspui/handle/1/19403-
dc.language.isoeng-
dc.titleCorrigendum to "Childhood-onset generalized epilepsy in Bainbridge-Ropers syndrome" [Epilepsy Res. 140 (2018) 166-170].-
dc.typeJournal Article-
dc.identifier.journaltitleEpilepsy research-
dc.identifier.affiliationDepartment of Paediatrics, The University of Melbourne, Parkville, Victoria, Australiaen
dc.identifier.affiliationInstitute of Medical Genetics, University Hospital of Wales, Heath Park Way, Cardiff, UKen
dc.identifier.affiliationDivision of Cancer and Genetics, School of Medicine, Cardiff University, Cardiff, UKen
dc.identifier.affiliationSheffield Clinical Genetics Service, Sheffield Children's NHS Foundation Trust, Herries Road, Sheffield, UKen
dc.identifier.affiliationAcademic Unit of Child Health, University of Sheffield, Sheffield, UKen
dc.identifier.affiliationEpilepsy Research Centre, Department of Medicine, Austin Health, The University of Melbourne, Heidelberg, Victoria, Australiaen
dc.identifier.affiliationDepartment of Pediatrics, Faculty of Medicine, McGill University, Montreal, Quebec, Canadaen
dc.identifier.affiliationDivision of Child Neurology, Montreal Children's Hospital, McGill University Health Centre, 1001 Décarie Blvd., Montreal, Quebec, Canadaen
dc.identifier.affiliationVictorian Clinical Genetics Service, Murdoch Children's Research Institute, 50 Flemington Road, Parkville, Victoria, Australiaen
dc.identifier.affiliationDepartment of Neurology, Royal Children's Hospital, Parkville, Victoria, Australiaen
dc.identifier.affiliationManchester Centre for Genomic Medicine, Saint Mary's Hospital, Oxford Road, Manchester, UKen
dc.identifier.affiliationDivision of Evolution and Genomic Sciences, Faculty of Biology, Medicine and Health, University of Manchester, Oxford Road, Manchester, UKen
dc.identifier.affiliationSouth East Thames Regional Genetics Service, Guy's and St. Thomas' Hospital, Great Maze Pond, London, UK-
dc.identifier.affiliationDepartment of Paediatric Neurology, Neuromuscular Service, Evelina Children's Hospital, St. Thomas' Hospital, Westminster Bridge Road, London, UK-
dc.identifier.affiliationLeicester Clinical Genetics Service, University Hospitals of Leicester NHS Trust, Leicester, UK-
dc.identifier.affiliationThe Florey Institute of Neuroscience and Mental Health, Heidelberg, Victoria, Australia-
dc.identifier.doi10.1016/j.eplepsyres.2018.07.019-
dc.identifier.orcid0000-0001-7831-4593en
dc.identifier.orcid0000-0002-2311-2174en
dc.identifier.pubmedid30104120-
dc.type.austinPublished Erratum-
local.name.researcherScheffer, Ingrid E
item.fulltextNo Fulltext-
item.openairetypeJournal Article-
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
item.grantfulltextnone-
item.languageiso639-1en-
item.cerifentitytypePublications-
crisitem.author.deptEpilepsy Research Centre-
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