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A Ser252Trp Mutation in Fibroblast Growth Factor Receptor 2 (FGFR2) Mimicking Human Apert Syndrome Reveals an Essential Role for FGF Signaling in the Regulation of Endochondral Bone Formation
Chen P,
Zhang L,
Weng T,
Zhang S,
Sun S,
et al.
(2014)
A Ser252Trp Mutation in Fibroblast Growth Factor Receptor 2 (FGFR2) Mimicking Human Apert Syndrome Reveals an Essential Role for FGF Signaling in the Regulation of Endochondral Bone Formation.
PLOS ONE 9(1): e87311.
https://doi.org/10.1371/journal.pone.0087311