CHD7 regulates craniofacial cartilage development via controlling HTR2B expression
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DOI: 10.1093/jbmr/zjae024
Abstract: Abstract Mutations in the Chromodomain helicase DNA-binding protein 7 – coding gene (CHD7) cause CHARGE syndrome (CS). Although craniofacial and skeletal abnormalities are major features of CS patients, the role of CHD7 in bone and… read more here.
Keywords: cartilage development; craniofacial cartilage; cartilage; chd7 ... See more keywords