Heterozygous Variants in KMT2E Cause a Spectrum of Neurodevelopmental Disorders and Epilepsy

Published 2019 View Full Article

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Title
Heterozygous Variants in KMT2E Cause a Spectrum of Neurodevelopmental Disorders and Epilepsy
Authors
Keywords
KMT2E, global developmental delay, intellectual disability, epilepsy, epileptic encephalopathy, autism, neurodevelopmental disorder, H3K4 methylation
Journal
AMERICAN JOURNAL OF HUMAN GENETICS
Volume -, Issue -, Pages -
Publisher
Elsevier BV
Online
2019-05-10
DOI
10.1016/j.ajhg.2019.03.021

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