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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...
में बचाया:
| में प्रकाशित: | PLoS One |
|---|---|
| मुख्य लेखकों: | , , , |
| स्वरूप: | Artigo |
| भाषा: | Inglês |
| प्रकाशित: |
Public Library of Science
2015
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| विषय: | |
| ऑनलाइन पहुंच: | 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 |
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