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Published in 2020 at "Developmental Dynamics"
DOI: 10.1002/dvdy.239
Abstract: Apert syndrome is an autosomal, dominant inherited disorder characterized by craniosynostosis and syndactyly caused by gain‐of‐function mutations in the fibroblast growth factor receptor 2 (FGFR2) gene. Wnt/β‐catenin signaling plays critical roles in regulating the skeletal…
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Keywords:
model;
apert syndrome;
fgfr2s252w;
developing coronal ... See more keywords