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Mark Perfetto, Xiaolu Xu, Congyu Lu +5 more ยท 2021 ยท Development (Cambridge, England) ยท added 2026-04-24
Mutations in the RNA helicase DDX3 have emerged as a frequent cause of intellectual disability in humans. Because many individuals carrying DDX3 mutations have additional defects in craniofacial struc Show more
Mutations in the RNA helicase DDX3 have emerged as a frequent cause of intellectual disability in humans. Because many individuals carrying DDX3 mutations have additional defects in craniofacial structures and other tissues containing neural crest (NC)-derived cells, we hypothesized that DDX3 is also important for NC development. Using Show less
no PDF DOI: 10.1242/dev.184341
SNAI1