Autosomal dominant SCN8A mutation with an unusually mild phenotype

Published 2016 View Full Article

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Title
Autosomal dominant SCN8A mutation with an unusually mild phenotype
Authors
Keywords
SCN8A, Focal epilepsy, Voltage-gated sodium channels, Next generation sequence analysis, Benign familial infantile epilepsy
Journal
EUROPEAN JOURNAL OF PAEDIATRIC NEUROLOGY
Volume 20, Issue 5, Pages 761-765
Publisher
Elsevier BV
Online
2016-05-01
DOI
10.1016/j.ejpn.2016.04.015

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