Prospective signs of cleidocranial dysplasia in Cebpb deficiency

BACKGROUND: Although runt-related transcription factor 2 (RUNX2) has been considered a determinant of cleidocranial dysplasia (CCD), some CCD patients were free of RUNX2 mutations. CCAAT/enhancer-binding protein beta (Cebpb) is a key factor of Runx2 expression and our previous study has reported two...

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Detalles Bibliográficos
Autores principales: Huang, Boyen, Takahashi, Katsu, Jennings, Ernest A, Pumtang-on, Pongthorn, Kiso, Honoka, Togo, Yumiko, Saito, Kazuyuki, Sugai, Manabu, Akira, Shizuo, Shimizu, Akira, Bessho, Kazuhisa
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2014
Materias:
Research
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4039338/
https://www.ncbi.nlm.nih.gov/pubmed/24885110
http://dx.doi.org/10.1186/1423-0127-21-44

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4039338/
https://www.ncbi.nlm.nih.gov/pubmed/24885110
http://dx.doi.org/10.1186/1423-0127-21-44

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