How does genetic variation modify ND-CNV phenotypes?
Abstract
Rare copy-number variants (CNVs) associated with neurodevelopmental disorders (NDDs), i.e., ND-CNVs, provide an insight into the neurobiology of NDDs and, potentially, a link between biology and clinical outcomes. However, ND-CNVs are characterised by incomplete penetrance resulting in heterogeneous carrier phenotypes, ranging from non-affected to multimorbid psychiatric, neurological, and physical phenotypes. Recent evidence indicates that...
Paper Details
Title
How does genetic variation modify ND-CNV phenotypes?
Published Date
Feb 1, 2022
Journal
Volume
38
Issue
2
Pages
140 - 151
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