Spectrum of SCN8A-Related Epilepsy

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

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Bibliographic Details
Main Authors: Lindsey A Morgan (Author), John J Millichap (Author)
Format: Book
Published: Pediatric Neurology Briefs Publishers, 2015-02-01T00:00:00Z.
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3rd Floor Main Library

Holdings details from 3rd Floor Main Library
Call Number: A1234.567
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