Detection of a rare AXIN2 variant in an Iranian family with hypodontia and oligodontia
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...
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| Autori principali: | , , , , , |
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| Natura: | Artigo |
| Lingua: | Inglês |
| Pubblicazione: |
Tabriz University of Medical Sciences
2022-10-01
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| Serie: | Journal of Dental Research, Dental Clinics, Dental Prospects |
| Soggetti: | |
| Accesso online: | https://joddd.tbzmed.ac.ir/PDF/joddd-16-107.pdf |
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