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Brain Phenotypes in Two FGFR2 Mouse Models for Apert Syndrome
Apert syndrome (AS) is one of at least nine disorders considered members of the fibroblast growth factor receptor (FGFR) -1, -2, and -3–related craniosynostosis syndromes. Nearly 100% of individuals diagnosed with AS carry one of two neighboring mutations on Fgfr2. The cranial phenotype associated w...
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| Autors principals: | , , , , , , , , |
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| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
2010
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| Matèries: | |
| Accés en línia: | https://ncbi.nlm.nih.gov/pmc/articles/PMC2829947/ https://ncbi.nlm.nih.gov/pubmed/20077479 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/dvdy.22218 |
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