Screening PAX9, MSX1 and WNT10A Mutations in 4 Iranian Families with Non-Syndromic Tooth Agenesis

BACKGROUND: Tooth agenesis is one of the most common developmental anomalies in human and the main reasons for its occurrence are still unknown. Mutations of several genes such as PAX9, MSX1, AXIN2, KDF1 and WNT10A have been reported which are associated with non-syndromic tooth agenesis. However, P...

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Detalles Bibliográficos
Autores principales: Safari, Shiva, Ebadifar, Asghar, Najmabadi, Hossien, Kamali, Koorosh, Abedini, Seyedeh Sedigheh
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Avicenna Research Institute 2020
Materias:
Original Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7502159/
https://www.ncbi.nlm.nih.gov/pubmed/33014315

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7502159/
https://www.ncbi.nlm.nih.gov/pubmed/33014315

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