Genetic heterogeneity in familial forms of genetic generalized epilepsy: from mono- to oligogenism
Genetic heterogeneity in familial forms of genetic generalized epilepsy: from mono- to oligogenism
About this item
Full title
Author / Creator
Dahawi, Maha , de Sainte Agathe, Jean-Madeleine , Elmagzoub, Mohamed S. , Ahmed, Elhami A. , Buratti, Julien , Courtin, Thomas , Noé, Eric , Bogoin, Julie , Copin, Bruno , Elmugadam, Fatima A. , Abdelgadir, Wasma A. , Ahmed, Ahmed K. M. A. , Daldoum, Mohamed A. , Altayeb, Rayan Mamoon Ibrahim , Bashir, Mohamed , Khalid, Leena Mohamed , Gamil, Sahar , Baldassari, Sara , Elsayed, Liena , Keren, Boris , Nuel, Gregory , Ahmed, Ammar E. and Leguern, Eric
Publisher
England: BioMed Central Ltd
Journal title
Language
English
Formats
Publication information
Publisher
England: BioMed Central Ltd
Subjects
More information
Scope and Contents
Contents
Genetic generalized epilepsy (GGE) including childhood absence epilepsy, juvenile absence epilepsy, juvenile myoclonic epilepsy (JME), and GGE with tonic-clonic seizures (TCS) (GGE-TCS), is genetically influenced with a two- to four- fold increased risk in the first-degree relatives of patients. Since large families with GGE are very rare, internat...
Alternative Titles
Full title
Genetic heterogeneity in familial forms of genetic generalized epilepsy: from mono- to oligogenism
Authors, Artists and Contributors
Author / Creator
de Sainte Agathe, Jean-Madeleine
Elmagzoub, Mohamed S.
Ahmed, Elhami A.
Buratti, Julien
Courtin, Thomas
Noé, Eric
Bogoin, Julie
Copin, Bruno
Elmugadam, Fatima A.
Abdelgadir, Wasma A.
Ahmed, Ahmed K. M. A.
Daldoum, Mohamed A.
Altayeb, Rayan Mamoon Ibrahim
Bashir, Mohamed
Khalid, Leena Mohamed
Gamil, Sahar
Baldassari, Sara
Elsayed, Liena
Keren, Boris
Nuel, Gregory
Ahmed, Ammar E.
Leguern, Eric
Identifiers
Primary Identifiers
Record Identifier
TN_cdi_doaj_primary_oai_doaj_org_article_da14490885db477eb26406082e9daf33
Permalink
https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_doaj_primary_oai_doaj_org_article_da14490885db477eb26406082e9daf33
Other Identifiers
ISSN
1479-7364
E-ISSN
1479-7364
DOI
10.1186/s40246-024-00659-9
