Novel WNT10A variant in a Japanese case of nonsyndromic oligodontia

Congenital tooth agenesis is one of the most common anomalies in humans. Many genetic factors are involved in tooth development, including MSX1, PAX9, WNT10A, and LRP6. Thus, mutations in these genes can cause congenital tooth agenesis in humans. In this study, we identified a novel nonsense WNT10A...

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Detalles Bibliográficos
Autores principales: Adachi, Junya, Aoki, Yoshihiko, Izumi, Hiroto, Nishiyama, Takeshi, Nakayama, Atsuo, Sana, Masatoshi, Morimoto, Kyoko, Kaetsu, Atsuo, Shirozu, Takamasa, Osumi, Eriko, Matsuoka, Michiko, Hayakawa, Eri, Maeda, Nasel, Machida, Junichiro, Nagao, Toru, Tokita, Yoshihito
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2023
Materias:
Data Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9879990/
https://www.ncbi.nlm.nih.gov/pubmed/36702846
http://dx.doi.org/10.1038/s41439-023-00230-3

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9879990/
https://www.ncbi.nlm.nih.gov/pubmed/36702846
http://dx.doi.org/10.1038/s41439-023-00230-3

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