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Two novel mutations in MSX1 causing oligodontia
Tooth agenesis is one of the most common developmental anomalies in humans and can affect dental occlusion and speech pronunciation. Research has identified an association between mutations in MSX1, PAX9, EDA, AXIN2, WNT10A, WNT10B and LRP6 and human tooth agenesis. Two unrelated individuals with no...
Sparad:
| I publikationen: | PLoS One |
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| Huvudupphovsmän: | , , , |
| Materialtyp: | Artigo |
| Språk: | Inglês |
| Publicerad: |
Public Library of Science
2020
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| Ämnen: | |
| Länkar: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6948825/ https://ncbi.nlm.nih.gov/pubmed/31914153 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1371/journal.pone.0227287 |
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