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pro vyhledávání: '"Xianding Sun"'
Autor:
Wei, Xu, Fengtao, Luo, Quan, Wang, Qiaoyan, Tan, Junlan, Huang, Siru, Zhou, Zuqiang, Wang, Xianding, Sun, Liang, Kuang, Min, Jin, Nan, Su, Wanling, Jiang, Liang, Chen, Huabing, Qi, Ying, Zhu, Bo, Chen, Hangang, Chen, Shuai, Chen, Yu, Gao, Xiaoling, Xu, Chuxia, Deng, Lin, Chen, Yangli, Xie, Xiaolan, Du
Publikováno v:
Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research. 32(11)
Apert syndrome is one of the most severe craniosynostoses, resulting from gain-of-function mutations in fibroblast growth factor receptor 2 (FGFR2). Previous studies have shown that gain-of-function mutations of FGFR2 (S252W or P253R) cause skull mal