Cargando…
A Novel AXIN2 Missense Mutation Is Associated with Non-Syndromic Oligodontia
Oligodontia is defined as the congenital absence of six or more permanent teeth, excluding the third molars. Oligodontia may contribute to masticatory dysfunction, speech alteration, aesthetic problems and malocclusion. Numerous gene mutations have been association with oligodontia. In the present s...
| Autores principales: | , , , |
|---|---|
| Formato: | Online Artículo Texto |
| Lenguaje: | English |
| Publicado: |
Public Library of Science
2015
|
| Materias: | |
| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4583461/ https://www.ncbi.nlm.nih.gov/pubmed/26406231 http://dx.doi.org/10.1371/journal.pone.0138221 |