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

• Главные авторы: Shiva Safari (Автор), Asghar Ebadifar (Автор), Hossien Najmabadi (Автор), Koorosh Kamali (Автор), Seyedeh Sedigheh Abedini (Автор), Mohammad Mousavi (Автор)
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• Опубликовано: Tabriz University of Medical Sciences, 2022-10-01T00:00:00Z.
• Предметы: article
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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...