Calcium Channel Defects in Models of Inherited Generalized Epilepsy
Author:
Publisher
Wiley
Subject
Clinical Neurology,Neurology
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1528-1157.2000.tb00305.x/fullpdf
Reference10 articles.
1. Absence Epilepsy in Tottering Mutant Mice Is Associated with Calcium Channel Defects
2. Mutation of the Ca2+ Channel β Subunit Gene Cchb4 Is Associated with Ataxia and Seizures in the Lethargic (lh) Mouse
3. The mouse stargazer gene encodes a neuronal Ca2+-channel γ subunit
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