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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
- Peng Chen,
- Li Zhang,
- Tujun Weng,
- Shichang Zhang,
- Shijin Sun,
- Mingtao Chang,
- Yang Li,
- Bo Zhang,
- Lianyang Zhang
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- Published: January 28, 2014
- https://doi.org/10.1371/journal.pone.0087311