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Stogmann, E.* ; Lichtner, P. ; Baumgartner, C.* ; Schmied, M.* ; Hotzy, C.* ; Asmus, F.* ; Leutmezer, F.* ; Bonelli, S.* ; Assem-Hilger, E. ; Vass, K.* ; Hatala, K.* ; Strom, T.M. ; Meitinger, T. ; Zimprich, F.* ; *

Mutations in the CLCN2 gene are a rare cause of idiopathic generalized epilepsy syndromes.

Neurogenetics 7, 265-268 (2006)
DOI
Open Access Green möglich sobald Postprint bei der ZB eingereicht worden ist.
Mutations in the chloride channel gene CLCN2 have been reported in families with generalized and focal epilepsy syndromes. To evaluate the contribution of mutations in the CLCN2 gene to the etiology of epilepsies in our population, we screened 96 patients with different epilepsy syndromes and a putative genetic background. No definite mutations were found in our study population. We conclude that mutations in the CLCN2 gene are only a rare cause of idiopathic generalized epilepsy. © Springer-Verlag 2006.
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Publikationstyp Artikel: Journalartikel
Dokumenttyp Wissenschaftlicher Artikel
Korrespondenzautor
Schlagwörter CLCN2; idiopathic generalized epilepsy
ISSN (print) / ISBN 1364-6745
e-ISSN 1364-6753
Zeitschrift Neurogenetics
Quellenangaben Band: 7, Heft: 4, Seiten: 265-268 Artikelnummer: , Supplement: ,
Verlag Springer
Nichtpatentliteratur Publikationen
Begutachtungsstatus Peer reviewed
Institut(e) Institute of Human Genetics (IHG)