Disruption of an EHMT1-Associated Chromatin-Modification Module Causes Intellectual Disability
Abstract
Intellectual disability (ID) disorders are genetically and phenotypically highly heterogeneous and present a major challenge in clinical genetics and medicine. Although many genes involved in ID have been identified, the etiology is unknown in most affected individuals. Moreover, the function of most genes associated with ID remains poorly characterized. Evidence is accumulating that the control of gene transcription through epigenetic...
Paper Details
Title
Disruption of an EHMT1-Associated Chromatin-Modification Module Causes Intellectual Disability
Published Date
Jul 1, 2012
Volume
91
Issue
1
Pages
73 - 82
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