Evaluation of vitamin D receptor (VDR) gene polymorphisms (FokI, TaqI and ApaI) in a family with dentinogenesis imperfecta

Dentinogenesis imperfecta Type II (DGI-II) is a condition inherited as an autosomal dominant trait and characterized by abnormal dentine structure affecting both the primary and secondary dentitions. The genetic etiology of the disease still remains unclear, suggesting a genetically heterogeneous ba...

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Veröffentlicht in:	Cytology and genetics 2013-09, Vol.47 (5), p.282-286
Hauptverfasser:	Ulucan, K., Akyüz, S., Özbay, G., Pekiner, F. N., İlter Güney, A.
Format:	Artikel
Sprache:	eng
Schlagworte:	Biomedical and Life Sciences Biomedicine Human Genetics
Online-Zugang:	Volltext
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