De novo SCN1A mutations in Dravet syndrome and related epileptic encephalopathies are largely of paternal origin

Published 2009 View Full Article

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Title
De novo SCN1A mutations in Dravet syndrome and related epileptic encephalopathies are largely of paternal origin
Authors
Keywords
-
Journal
JOURNAL OF MEDICAL GENETICS
Volume 47, Issue 2, Pages 137-141
Publisher
BMJ
Online
2009-07-10
DOI
10.1136/jmg.2008.065912

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