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

• Egile Nagusiak: Shiva Safari (Egilea), Asghar Ebadifar (Egilea), Hossien Najmabadi (Egilea), Koorosh Kamali (Egilea), Seyedeh Sedigheh Abedini (Egilea), Mohammad Mousavi (Egilea)
• Formatua: Liburua
• Argitaratua: Tabriz University of Medical Sciences, 2022-10-01T00:00:00Z.
• Gaiak: article
• Sarrera elektronikoa: 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...