POGZ truncating alleles cause syndromic intellectual disability
Abstract
Large-scale cohort-based whole exome sequencing of individuals with neurodevelopmental disorders (NDDs) has identified numerous novel candidate disease genes; however, detailed phenotypic information is often lacking in such studies. De novo mutations in pogo transposable element with zinc finger domain (POGZ) have been identified in six independent and diverse cohorts of individuals with NDDs ranging from autism spectrum disorder to...
Paper Details
Title
POGZ truncating alleles cause syndromic intellectual disability
Published Date
Jan 6, 2016
Journal
Volume
8
Issue
1
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