The American Journal of Human Genetics
Volume 100, Issue 1, 5 January 2017, Pages 128-137
ReportA Syndromic Neurodevelopmental Disorder Caused by De Novo Variants in EBF3
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Keywords
Drosophila
knot
ataxia
hypotonia
intellectual disability
expressive speech disorder
COE3
transcription factor
vermian hypoplasia
inhibitory GABAergic neurons
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These authors contributed equally to this work
© 2016 American Society of Human Genetics.