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...
Veröffentlicht in: | Zhonghua er ke za zhi = Chinese journal of pediatrics. - 1960. - 43(2005), 2 vom: 18. Feb., Seite 133-6 |
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1. Verfasser: | |
Weitere Verfasser: | , , , , , , , , , , |
Format: | Aufsatz |
Sprache: | Chinese |
Veröffentlicht: |
2005
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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 |