Please use this identifier to cite or link to this item: https://ahro.austin.org.au/austinjspui/handle/1/11248
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dc.contributor.authorKlein, K Men
dc.contributor.authorYendle, S Cen
dc.contributor.authorHarvey, A Simonen
dc.contributor.authorAntony, J Hen
dc.contributor.authorWallace, Gen
dc.contributor.authorBienvenu, Ten
dc.contributor.authorScheffer, Ingrid Een
dc.date.accessioned2015-05-16T00:50:13Z
dc.date.available2015-05-16T00:50:13Z
dc.date.issued2011-04-19en
dc.identifier.citationNeurology; 76(16): 1436-8en
dc.identifier.govdoc21502606en
dc.identifier.otherPUBMEDen
dc.identifier.urihttps://ahro.austin.org.au/austinjspui/handle/1/11248en
dc.language.isoenen
dc.subject.otherChild, Preschoolen
dc.subject.otherDNA Mutational Analysisen
dc.subject.otherFemaleen
dc.subject.otherHumansen
dc.subject.otherInfanten
dc.subject.otherMuscle Hypertonia.etiology.geneticsen
dc.subject.otherMutation.geneticsen
dc.subject.otherProtein-Serine-Threonine Kinases.geneticsen
dc.subject.otherSeizures.complications.geneticsen
dc.titleA distinctive seizure type in patients with CDKL5 mutations: Hypermotor-tonic-spasms sequence.en
dc.typeJournal Articleen
dc.identifier.journaltitleNeurologyen
dc.identifier.affiliationEpilepsy Research Centre, Neuroscience Building, Heidelberg Repatriation Hospital, West Heidelberg, Victoria 3081, Australiaen
dc.identifier.doi10.1212/WNL.0b013e3182166e58en
dc.description.pages1436-8en
dc.relation.urlhttps://pubmed.ncbi.nlm.nih.gov/21502606en
dc.type.austinJournal Articleen
local.name.researcherScheffer, Ingrid E
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
item.cerifentitytypePublications-
item.fulltextNo Fulltext-
item.grantfulltextnone-
item.languageiso639-1en-
item.openairetypeJournal Article-
crisitem.author.deptEpilepsy Research Centre-
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