A novel inherited SCN1A mutation associated with different neuropsychological phenotypes: Is there a common core deficit?

Published 2015 View Full Article

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Title
A novel inherited SCN1A mutation associated with different neuropsychological phenotypes: Is there a common core deficit?
Authors
Keywords
SCN1A, gene, Dravet syndrome spectrum, Neuropsychological phenotype
Journal
EPILEPSY & BEHAVIOR
Volume 43, Issue -, Pages 89-92
Publisher
Elsevier BV
Online
2015-01-07
DOI
10.1016/j.yebeh.2014.11.009

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