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Epilepsia eta Genetika

URTASUN, Miguel and POZA, Juan José and COBO, Ana María and AZPITARTE, Margarita and MARTÍ MASSÓ, José Félix and MARTÍNEZ-GIL, Ángel and BAUTISTA ESPINAL, Juan and CARRERA, Edurne and SÁENZ, Amets and LÓPEZ DE MUNAIN ARREGI, Adolfo (2006) Epilepsia eta Genetika. Osasunaz. Cuadernos de Ciencias Médicas (7). pp. 169-189. ISSN 1577-8533

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Official URL: http://www.euskomedia.org/analitica/10794


The isolating of certain genes that intervene in the origin of idiopathic epilepsy has allowed for a better classification of epilepsy as a whole. This work is about the clinical analysis of two families with an epileptic syndrome. The first family displays a nocturnal epilepsy associated to chromosome 20q, which has a mutation in gen (CHRNA4) of sub-unit á4 of the acetylcoline nicotinic receptor. The second family displays a dominant lateral temporal lobe and autosomal epilepsy associated to chromosome 10q.

Item Type:Article
Additional Information:Continuación de Cuadernos de Sección. Ciencias médicas
Uncontrolled Keywords:Medicina
Subjects:Medical Sciences
ID Code:7523
Last Modified:11 May 2011 16:45

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