PAX9 Polymorphisms and susceptibility with sporadic tooth agenesis in Turkish populations: a case-control study

BACKGROUND: Hypodontia, the congenital absence of one or a few teeth is one of the most common alterations of the human dentition. Familial hypodontia is caused by mutations in PAX9, Msx1 and Axin2 genes. Limited numbers of studies are present to show etiological factors beyond this anomaly in Turki...

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Detalles Bibliográficos
Autores principales: Isman, Eren, Nergiz, Suleyman, Acar, Hasan, Sari, Zafer
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2013
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3826669/
https://www.ncbi.nlm.nih.gov/pubmed/24160254
http://dx.doi.org/10.1186/1471-2164-14-733

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3826669/
https://www.ncbi.nlm.nih.gov/pubmed/24160254
http://dx.doi.org/10.1186/1471-2164-14-733

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