Published 2015 | Version v1.0.0
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Spectrum of SCN8A-Related Epilepsy

Abstract

Investigators from the EuroEPINOMICS European research consortium studied 17 patients with epileptic encephalopathy due to SCN8A mutations and reported the specific genetic and phenotypic features.

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PNB-29-16

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Created
2015
When the item was originally created.