Please use this identifier to cite or link to this item: https://ahro.austin.org.au/austinjspui/handle/1/11695
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dc.contributor.authorHildebrand, Michael Sen
dc.contributor.authorDahl, Hans-Henrik Men
dc.contributor.authorDamiano, John Anthonyen
dc.contributor.authorSmith, Richard J Hen
dc.contributor.authorScheffer, Ingrid Een
dc.contributor.authorBerkovic, Samuel Fen
dc.date.accessioned2015-05-16T01:18:47Z
dc.date.available2015-05-16T01:18:47Z
dc.date.issued2013-03-06en
dc.identifier.citationJournal of Medical Genetics 2013; 50(5): 271-9en
dc.identifier.govdoc23468209en
dc.identifier.otherPUBMEDen
dc.identifier.urihttps://ahro.austin.org.au/austinjspui/handle/1/11695en
dc.description.abstractRecent advances in molecular genetics have translated into the increasing utilisation of genetic testing in the routine clinical practice of neurologists. There has been a steady, incremental increase in understanding the genetic variation associated with epilepsies. Genetic testing in the epilepsies is not yet widely practiced, but the advent of new screening technologies promises to exponentially expand both knowledge and clinical utility. To maximise the value of this new genetic insight we need to rapidly extrapolate genetic findings to inform patients of their diagnosis, prognosis, recurrence risk and the clinical management options available for their specific genetic condition. Comprehensive, highly specific and sensitive genetic test results improve the management of patients by neurologists and clinical geneticists. Here we discuss the latest developments in clinical genetic testing for epilepsy and describe new molecular genetics platforms that will transform both genetic screening and novel gene discovery.en
dc.language.isoenen
dc.subject.otherDNA Copy Number Variationsen
dc.subject.otherEpilepsy.geneticsen
dc.subject.otherGenetic Predisposition to Disease.geneticsen
dc.subject.otherGenetic Testing.methods.trendsen
dc.subject.otherGenetic Variationen
dc.subject.otherHigh-Throughput Nucleotide Sequencing.methodsen
dc.subject.otherHumansen
dc.subject.otherMolecular Biology.methods.trendsen
dc.subject.otherMultifactorial Inheritance.geneticsen
dc.subject.otherMutation.geneticsen
dc.titleRecent advances in the molecular genetics of epilepsy.en
dc.typeJournal Articleen
dc.identifier.journaltitleJournal of medical geneticsen
dc.identifier.affiliationDepartment of Medicine, Epilepsy Research Centre, University of Melbourne, Melbourne Brain Centre, Austin Health, 275 Burgundy Street, Heidelberg, Victoria 3084, Australiaen
dc.identifier.doi10.1136/jmedgenet-2012-101448en
dc.description.pages271-9en
dc.relation.urlhttps://pubmed.ncbi.nlm.nih.gov/23468209en
dc.type.austinJournal Articleen
local.name.researcherBerkovic, Samuel F
item.grantfulltextnone-
item.openairetypeJournal Article-
item.languageiso639-1en-
item.fulltextNo Fulltext-
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
item.cerifentitytypePublications-
crisitem.author.deptEpilepsy Research Centre-
crisitem.author.deptMedicine (University of Melbourne)-
crisitem.author.deptEpilepsy Research Centre-
crisitem.author.deptEpilepsy Research Centre-
crisitem.author.deptNeurology-
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