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An Fgfr3-activating mutation in immature murine osteoblasts affects the appendicular and craniofacial skeleton
Achondroplasia (ACH), the most common form of dwarfism, is caused by a missense mutation in the gene coding for fibroblast growth factor receptor 3 (FGFR3). The resulting increase in FGFR3 signaling perturbs the proliferation and differentiation of chondrocytes (CCs), alters the process of endochond...
Guardat en:
| Publicat a: | Dis Model Mech |
|---|---|
| Autors principals: | , , , , , |
| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
The Company of Biologists Ltd
2021
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| Matèries: | |
| Accés en línia: | https://ncbi.nlm.nih.gov/pmc/articles/PMC8084574/ https://ncbi.nlm.nih.gov/pubmed/33737326 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1242/dmm.048272 |
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