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 (Q37525589)
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scientific article published on 28 January 2014
| Language | Label | Description | Also known as |
|---|---|---|---|
| English | 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 |
scientific article published on 28 January 2014 |
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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 (English)
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Peng Chen
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Li Zhang
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Tujun Weng
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Shichang Zhang
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Shijin Sun
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Mingtao Chang
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Yang Li
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Bo Zhang
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Lianyang Zhang
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28 January 2014
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e87311
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28 January 2014
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