An inherited FGFR2 mutation increased osteogenesis gene expression and result in Crouzon syndrome

BACKGROUND: FGFR2 encodes a fibroblast growth factor receptor whose mutations are responsible for the Crouzon syndrome, involving craniosynostosis and facial dysostosis with shallow orbits. However, few reports are available quantifying the orbital volume of Crouzon syndrome and there was little dir...

Descripción completa

Detalles Bibliográficos
Autores principales: Fan, Jiayan, Li, Yinwei, Jia, Renbing, Fan, Xianqun
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2018
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5975660/
https://www.ncbi.nlm.nih.gov/pubmed/29848297
http://dx.doi.org/10.1186/s12881-018-0607-8

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5975660/
https://www.ncbi.nlm.nih.gov/pubmed/29848297
http://dx.doi.org/10.1186/s12881-018-0607-8

Ejemplares similares