Filling in the gaps in cranial suture biology

Research output: Contribution to journalArticlepeer-review

Abstract

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.
Original languageEnglish
Pages (from-to)231-232
Number of pages2
JournalNature Genetics
Volume45
Issue number3
DOIs
Publication statusPublished - Mar 2013

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