Please use this identifier to cite or link to this item: https://ahro.austin.org.au/austinjspui/handle/1/28330
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dc.contributor.authorGooley, Samuel-
dc.contributor.authorCrompton, Douglas E-
dc.contributor.authorBerkovic, Samuel F-
dc.date2021-12-08-
dc.date.accessioned2021-12-14T03:12:46Z-
dc.date.available2021-12-14T03:12:46Z-
dc.date.issued2021-12-08-
dc.identifier.citationEpileptic Disorders 2021; online first: 8 Decemberen
dc.identifier.urihttps://ahro.austin.org.au/austinjspui/handle/1/28330-
dc.description.abstractThere are a number of familial focal epilepsy syndromes, each with distinct clinical characteristics. Here, we review the epilepsy phenotypes and the genetic architecture of these syndromes. Using an illustrative clinical case, we describe the important steps in making a diagnosis and ordering appropriate genetic tests. Our discussion on the genetics of the familial focal epilepsies will provide a framework for interpreting the results of genetic testing, and allow us to apply this information to patient management.en
dc.language.isoeng-
dc.subjectDEPDC5en
dc.subjectGRIN2Aen
dc.subjectLGI1en
dc.subjectfamilial focal epilepsyen
dc.subjectfocal epilepsy geneticsen
dc.subjectmTORen
dc.titleILAE Genetic Literacy Series: familial focal epilepsy syndromes.en
dc.typeJournal Articleen
dc.identifier.journaltitleEpileptic Disordersen
dc.identifier.affiliationDepartment of Neurology, Northern Health, Epping, Victoria 3076, Australiaen
dc.identifier.affiliationEpilepsy Research Centreen
dc.identifier.doi10.1684/epd.2021.1393en
dc.type.contentTexten
dc.identifier.pubmedid34887240-
local.name.researcherBerkovic, Samuel F
item.languageiso639-1en-
item.openairetypeJournal Article-
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
item.fulltextNo Fulltext-
item.grantfulltextnone-
item.cerifentitytypePublications-
crisitem.author.deptEpilepsy Research Centre-
crisitem.author.deptNeurology-
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