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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...
| Autores principales: | , , , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
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BioMed Central
2013
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| 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 |