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

• Main Authors: Shiva Safari (Author), Asghar Ebadifar (Author), Hossien Najmabadi (Author), Koorosh Kamali (Author), Seyedeh Sedigheh Abedini (Author), Mohammad Mousavi (Author)
• Format: Book
• Published: Tabriz University of Medical Sciences, 2022-10-01T00:00:00Z.
• Subjects: article
• Online Access: 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...