Functional analysis of novel DEAF1 variants identified through clinical exome sequencing expands DEAF1 -associated neurodevelopmental disorder (DAND) phenotype

Published 2017 View Full Article

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Keywords

Journal

HUMAN MUTATION

Volume 38, Issue 12, Pages 1774-1785

Publisher

Wiley

Online

2017-09-22

DOI

10.1002/humu.23339

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