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Published in 2019 at "JCI insight"
DOI: 10.1172/jci.insight.129380
Abstract: Kabuki syndrome 1 (KS1) is a Mendelian disorder of the epigenetic machinery caused by mutations in the gene encoding KMT2D, which methylates lysine 4 on histone H3 (H3K4). KS1 is characterized by intellectual disability, postnatal…
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Keywords:
chondrocyte differentiation;
kabuki syndrome;
precocious chondrocyte;
chondrocyte ... See more keywords