Last updated on January 2019

Neuronal Excitability of HCN1 Channel Mutations in Dravet Syndrome


Brief description of study

This study addresses the changes in the axonal excitability parameters. It will compare these changes in patients with early infantile epileptic encephalopathy with HCN1 channel mutation and in control patients, with and without epilepsy.

Clinical Study Identifier: NCT02896608

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Recruitment Status: Open


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