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Chromatin remodeling genes in CHD. A Chromatin remodeling genes with mutations identified in CHD patients to date, highlighting the overlap between CHD and NDD genes. Nucleosomes with H3K4, H3K9, H3K27, H3K36 and H4K20 methylation and/or acetylation, and H2BK120 ubiquitylation are shown (adapted from Homsy et al, Science 2015). B Syndromes associated with chromatin remodeling gene mutations and their associated CHD and neurodevelopmental abnormalities.
