GLUT1 mutations are a rare cause of familial idiopathic generalized epilepsy.

Objective: The idiopathic generalized epilepsies (IGE) are the most common genetically determined epilepsies. However, the underlying genes are largely unknown. We screened the SLC2A1 gene, encoding the glucose transporter type 1 (GLUT1), for mutations in a group of 95 European patients with familia...

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Publicado en:	Neurology Vol. 78; no. 8; pp. 557 - 563
Autores principales:	Striano P, Weber YG, Toliat MR, Schubert J, Leu C, Chaimana R, Baulac S, Guerrero R, LeGuern E, Lehesjoki AE, Polvi A, Robbiano A, Serratosa JM, Guerrini R, Nürnberg P, Sander T, Zara F, Lerche H, Marini C, Striano, P
Formato:	research Journal Article
Publicado:	Lippincott Williams & Wilkins 2/21/2012
Acceso en línea:	Ver este registro en EBSCOhost