Mutations and polymorphisms of the CLCN2 gene in idiopathic epilepsy
2004; Lippincott Williams & Wilkins; Volume: 63; Issue: 8 Linguagem: Inglês
10.1212/01.wnl.0000142093.94998.1a
ISSN1526-632X
AutoresDaniela D’Agostino, Matteo Bertelli, Silvia Gallo, S Cecchin, Elena Albiero, P Garofalo, Antonio Gambardella, J.-M. St. Hilaire, Hubert Kwieciński, E. Andermann, Massimo Pandolfo,
Tópico(s)Ion Transport and Channel Regulation
ResumoThe authors analyzed the CLCN2 chloride channel gene in 112 probands with familial epilepsy, detecting 18 common polymorphisms. Two brothers with generalized epilepsy and their asymptomatic father, and a father and son with focal epilepsy carried variants of possible functional significance that were not found in 192 controls. The authors conclude that CLCN2 mutations may be a rare cause of familial epilepsy. Further studies are needed to test if polymorphisms in this gene are associated with epilepsy.
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