PRRT2 Mutations Cause Benign Familial Infantile Epilepsy and Infantile Convulsions with Choreoathetosis Syndrome

Published 2012 View Full Article

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Title
PRRT2 Mutations Cause Benign Familial Infantile Epilepsy and Infantile Convulsions with Choreoathetosis Syndrome
Authors
Keywords
-
Journal
AMERICAN JOURNAL OF HUMAN GENETICS
Volume 90, Issue 1, Pages 152-160
Publisher
Elsevier BV
Online
2012-01-13
DOI
10.1016/j.ajhg.2011.12.003

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