T-type calcium channel gene-CACNA1H is a susceptibility gene to childhood absence epilepsy

OBJECTIVE: Childhood absence epilepsy (CAE) is one of the most frequently recognized syndromes among the idiopathic generalized epilepsies (IGEs). It is considered to be a hereditary disease. The possible inheritance pattern of CAE is polygenic. The genes responsible for CAE, however, have not yet b...

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Bibliographische Detailangaben
Veröffentlicht in:Zhonghua er ke za zhi = Chinese journal of pediatrics. - 1960. - 43(2005), 2 vom: 18. Feb., Seite 133-6
1. Verfasser: Lü, Jian-jun (VerfasserIn)
Weitere Verfasser: Zhang, Yue-hua, Chen, Yu-cai, Pan, Hong, Wang, Ju-li, Zhang, Lei, Wu, Hu-sheng, Xu, Ke-ming, Liu, Xiao-yan, Tao, La-di, Shen, Yan, Wu, Xi-ru
Format: Aufsatz
Sprache:Chinese
Veröffentlicht: 2005
Zugriff auf das übergeordnete Werk:Zhonghua er ke za zhi = Chinese journal of pediatrics
Schlagworte:English Abstract Journal Article Research Support, Non-U.S. Gov't CACNA1H protein, human Calcium Channels, T-Type