Published 2007 | Version v1.0.0
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Infantile Epileptic Encephalopathies

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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PNB-21-25

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Created
2007
When the item was originally created.