De novo mutations in CSNK2A1 are associated with neurodevelopmental abnormalities and dysmorphic features

Title
De novo mutations in CSNK2A1 are associated with neurodevelopmental abnormalities and dysmorphic features
Authors
Keywords
Intellectual Disability, Neurodevelopmental Disorder, Missense Variant, Dysmorphic Feature, Whole Exome Sequencing
Journal
HUMAN GENETICS
Volume 135, Issue 7, Pages 699-705
Publisher
Springer Nature
Online
2016-04-05
DOI
10.1007/s00439-016-1661-y

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