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Mutations in theCLCN2gene are a rare cause of idiopathic generalized epilepsy syndromes

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

Publisher: Springer
Year: 2006
Tongue: English
Weight: 94 KB
Volume: 7
Category: Article
ISSN: 1364-6745
DOI: 10.1007/s10048-006-0057-x

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