Crouzon syndrome mouse model exhibits cartilage hyperproliferation and defective segmentation in the

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Crouzon syndrome is the result of a gain-of-function point mutation in FGFR2. Mimicking the human mutation, a mouse model of Crouzon syndrome(Fgfr2342Y) recapitulates patient deformities, including failed tracheal cartilage segmentation, resulting in a ca
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