A carregar...
Crouzon syndrome: Genetic and intervention review
Crouzon syndrome exhibits considerable phenotypic heterogeneity, in the aetiology of which genetics play an important role. FGFR2 mediates extracellular signals into cells and the mutations in the FGFR2 gene cause this syndrome occurrence. Activated FGFs/FGFR2 signaling disrupts the balance of diffe...
Na minha lista:
| Publicado no: | J Oral Biol Craniofac Res |
|---|---|
| Main Authors: | , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Elsevier
2019
|
| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6128172/ https://ncbi.nlm.nih.gov/pubmed/30202723 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.jobcr.2018.08.007 |
| Tags: |
Adicionar Tag
Sem tags, seja o primeiro a adicionar uma tag!
|