Detection of a rare AXIN2 variant in an Iranian family with hypodontia and oligodontia

• Κύριοι συγγραφείς: Shiva Safari (Συγγραφέας), Asghar Ebadifar (Συγγραφέας), Hossien Najmabadi (Συγγραφέας), Koorosh Kamali (Συγγραφέας), Seyedeh Sedigheh Abedini (Συγγραφέας), Mohammad Mousavi (Συγγραφέας)
• Μορφή: Βιβλίο
• Έκδοση: Tabriz University of Medical Sciences, 2022-10-01T00:00:00Z.
• Θέματα: article
• Διαθέσιμο Online: Connect to this object online.

Background. Hypodontia, or the absence of one or more teeth during tooth formation, is a highly prevalent dental anomaly. Nevertheless, the main causes are still unknown. Mutations in PAX9, MSX1, WNT10A, and AXIN2 genes are most commonly associated with non-syndromic tooth agenesis in the literature...