A Pro253Arg mutation in fibroblast growth factor receptor 2 (Fgfr2) causes skeleton malformation mimicking human Apert syndrome by affecting both chondrogenesis and osteogenesis
Titel:
A Pro253Arg mutation in fibroblast growth factor receptor 2 (Fgfr2) causes skeleton malformation mimicking human Apert syndrome by affecting both chondrogenesis and osteogenesis
Auteur:
Yin, Liangjun Du, Xiaolan Li, Cuiling Xu, Xiaoling Chen, Zhi Su, Nan Zhao, Ling Qi, Huabing Li, Fubing Xue, Jing Yang, Jing Jin, Min Deng, Chuxia Chen, Lin