Mutations in LGI1 cause autosomal-dominant partial epilepsy with auditory features
Mutations in LGI1 cause autosomal-dominant partial epilepsy with auditory features
About this item
Full title
Author / Creator
Kalachikov, Sergey , Evgrafov, Oleg , Ross, Barbara , Winawer, Melodie , Barker-Cummings, Christie , Boneschi, Filippo Martinelli , Choi, Chang , Morozov, Pavel , Das, Kamna , Teplitskaya, Elita , Yu, Andrew , Cayanis, Eftihia , Penchaszadeh, Graciela , Kottmann, Andreas H. , Pedley, Timothy A. , Hauser, W. Allen , Ottman, Ruth and Gilliam, T. Conrad
Publisher
New York: Nature Publishing Group US
Journal title
Language
English
Formats
Publication information
Publisher
New York: Nature Publishing Group US
Subjects
More information
Scope and Contents
Contents
The epilepsies are a common, clinically heterogeneous group of disorders defined by recurrent unprovoked seizures
1
. Here we describe identification of the causative gene in autosomal-dominant partial epilepsy with auditory features (ADPEAF, MIM 600512), a rare form of idiopathic lateral temporal lobe epilepsy characterized by partial seizur...
Alternative Titles
Full title
Mutations in LGI1 cause autosomal-dominant partial epilepsy with auditory features
Authors, Artists and Contributors
Author / Creator
Evgrafov, Oleg
Ross, Barbara
Winawer, Melodie
Barker-Cummings, Christie
Boneschi, Filippo Martinelli
Choi, Chang
Morozov, Pavel
Das, Kamna
Teplitskaya, Elita
Yu, Andrew
Cayanis, Eftihia
Penchaszadeh, Graciela
Kottmann, Andreas H.
Pedley, Timothy A.
Hauser, W. Allen
Ottman, Ruth
Gilliam, T. Conrad
Identifiers
Primary Identifiers
Record Identifier
TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_2606053
Permalink
https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_2606053
Other Identifiers
ISSN
1061-4036
E-ISSN
1546-1718
DOI
10.1038/ng832
