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

Author： 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.   Meitinger T.   Zimprich F.   Zimprich A.  

Publisher： Springer Publishing Company

ISSN： 1364-6745

Source： Neurogenetics, Vol.7, Iss.4, 2006-11, pp. : 265-268

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