SCN2A mutation associated with neonatal epilepsy, late-onset episodic ataxia, myoclonus, and pain

Published 2010 View Full Article

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Title
SCN2A mutation associated with neonatal epilepsy, late-onset episodic ataxia, myoclonus, and pain
Authors
Keywords
-
Journal
NEUROLOGY
Volume 75, Issue 16, Pages 1454-1458
Publisher
Ovid Technologies (Wolters Kluwer Health)
Online
2010-10-19
DOI
10.1212/wnl.0b013e3181f8812e

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