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...

Fuld beskrivelse

Na minha lista:
Bibliografiske detaljer
Udgivet i:PLoS One
Main Authors: Liu, Haochen, Ding, Tingting, Zhan, Yuan, Feng, Hailan
Format: Artigo
Sprog:Inglês
Udgivet: Public Library of Science 2015
Fag:
Research Article
Online adgang:https://ncbi.nlm.nih.gov/pmc/articles/PMC4583461/
https://ncbi.nlm.nih.gov/pubmed/26406231
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1371/journal.pone.0138221
Tags: Tilføj Tag
Ingen Tags, Vær først til at tagge denne postø!

Lignende værker