De novo GRIN1 mutations: An emerging cause of severe early infantile encephalopathy

Published 2017 View Full Article

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Title
De novo GRIN1 mutations: An emerging cause of severe early infantile encephalopathy
Authors
Keywords
GRIN1, Early onset encephalopathy, Oculogyric movements, De novo mutation
Journal
European Journal of Medical Genetics
Volume 60, Issue 6, Pages 317-320
Publisher
Elsevier BV
Online
2017-04-05
DOI
10.1016/j.ejmg.2017.04.001

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