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FAM20A is Essential for Amelogenesis, but is Dispensable for Dentinogenesis
Mutations in the gene encoding family with sequence similarity 20, member A (FAM20A) caused amelogenesis imperfecta (AI), in humans. However, the roles of FAM20A in amelogenesis and dentinogenesis are poorly understood. In this study, we generated a Fam20a knockout (Sox2-Cre;Fam20a(fl/fl)) mouse mod...
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| Publicat a: | J Mol Histol |
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| Autors principals: | , , , , , , |
| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
2019
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| Matèries: | |
| Accés en línia: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6861166/ https://ncbi.nlm.nih.gov/pubmed/31667691 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1007/s10735-019-09851-x |
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