A set of regulatory genes co-expressed in embryonic human brain is implicated in disrupted speech development

Volume: 24, Issue: 7, Pages: 1065 - 1078
Published: Feb 20, 2018
Abstract
Genetic investigations of people with impaired development of spoken language provide windows into key aspects of human biology. Over 15 years after FOXP2 was identified, most speech and language impairments remain unexplained at the molecular level. We sequenced whole genomes of nineteen unrelated individuals diagnosed with childhood apraxia of speech, a rare disorder enriched for causative mutations of large effect. Where DNA was available...
Paper Details
Title
A set of regulatory genes co-expressed in embryonic human brain is implicated in disrupted speech development
Published Date
Feb 20, 2018
Volume
24
Issue
7
Pages
1065 - 1078
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