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A soluble form of fibroblast growth factor receptor 2 (FGFR2) with S252W mutation acts as an efficient inhibitor for the enhanced osteoblastic differentiation caused by FGFR2 activation in Apert syndrome

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Description scientific article published on 13 August 2004
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author: Toshio Matsumoto 

Publication date August 13, 2004
Language English
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