A CACNB4 mutation shows that altered Cav2.1 function may be a genetic modifier of severe myoclonic epilepsy in infancy

Published 2008 View Full Article

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Title
A CACNB4 mutation shows that altered Cav2.1 function may be a genetic modifier of severe myoclonic epilepsy in infancy
Authors
Keywords
-
Journal
NEUROBIOLOGY OF DISEASE
Volume 32, Issue 3, Pages 349-354
Publisher
Elsevier BV
Online
2008-08-04
DOI
10.1016/j.nbd.2008.07.017

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