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...

Descripción completa

Detalles Bibliográficos
Autores principales: Safari, Shiva, Ebadifar, Asghar, Najmabadi, Hossien, Kamali, Koorosh, Abedini, Seyedeh Sedigheh, Mousavi, Mohammad
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Tabriz University of Medical Sciences 2022
Materias:
Original Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9763662/
https://www.ncbi.nlm.nih.gov/pubmed/36561383
http://dx.doi.org/10.34172/joddd.2022.018

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9763662/
https://www.ncbi.nlm.nih.gov/pubmed/36561383
http://dx.doi.org/10.34172/joddd.2022.018

Ejemplares similares