Please use this identifier to cite or link to this item: https://ahro.austin.org.au/austinjspui/handle/1/9150
Title: Genetics of the epilepsies.
Austin Authors: Berkovic, Samuel F ;Scheffer, Ingrid 
Affiliation: Epilepsy Research Institute, University of Melbourne, Austin and Repatriation Medical Centre, Australia
Issue Date: 1-Apr-1999
Publication information: Current Opinion in Neurology; 12(2): 177-82
Abstract: Epilepsies, like other common diseases, have complex inheritance, and molecular genetic studies in such conditions are difficult. There has been recent success in identifying the molecular basis of certain epilepsies, particularly in those syndromes with autosomal dominant inheritance. All four genes discovered to date for idiopathic epilepsies code for ion channel subunits, either ligand-gated or voltage-gated. The idiopathic epilepsies thus appear, at least in part, to be a family of channelopathies.
Gov't Doc #: 10226750
URI: http://ahro.austin.org.au/austinjspui/handle/1/9150
DOI: 10.1097/00019052-199904000-00008
URL: https://pubmed.ncbi.nlm.nih.gov/10226750
Type: Journal Article
Subjects: Epilepsy.genetics
Genetic Linkage
Genetics, Medical.methods.trends
Humans
Ion Channels.genetics
Molecular Biology.methods.trends
Mutation
Appears in Collections:Journal articles

Show full item record

Page view(s)

6
checked on Nov 28, 2022

Google ScholarTM

Check


Items in AHRO are protected by copyright, with all rights reserved, unless otherwise indicated.