Two new loci for premature fusion of the cranial sutures in humans suggest a common endpoint in osteoblast regulation, linking upregulation of phosphorylated ERK1/2 and TWIST1 haploinsufficiency.
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FitzPatrick, D. Filling in the gaps in cranial suture biology. Nat Genet 45, 231–232 (2013). https://doi.org/10.1038/ng.2557
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DOI: https://doi.org/10.1038/ng.2557
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