Infantile Epileptic Encephalopathies

Authors

  • J Gordon Millichap Northwestern University Feinberg School of Medicine

DOI:

https://doi.org/10.15844/pedneurbriefs-21-4-1

Keywords:

SMEI-Borderland, Myoclonic-Astatic Epilepsy, Dravet Syndrome

Abstract

The phenotypic variability associated with sodium channel alpha 1 subunit gene SCN1A mutations was studied in 188 patients with various infantile epileptic encephalopathies referred to the Universities of Adelaide and Melbourne, Australia; and centres in Glasgow, UK; Wellington, New Zealand; Montreal and Vancouver, Canada; Worcester, MD, USA, Israel, and Denmark.

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Published

2007-04-01

Issue

Vol 21, No 04 | Apr 2007

Section

Seizure Disorders

License

Copyright (c) 2007 The Author(s)

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