Publication | Closed Access
A pore mutation in a novel KQT-like potassium channel gene in an idiopathic epilepsy family
934
Citations
23
References
1998
Year
ChannelopathiesSignal TransductionHyperpolarization (Biology)NeurophysiologyGeneticsIdiopathic Epilepsy FamilyMolecular BiologyIon ChannelsElectrophysiologyMolecular NeurobiologyPore MutationMedicinePotassium HomeostasisSocial SciencesNeurogenetics
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