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The dentin phosphoprotein repeat region and inherited defects of dentin
Nonsyndromic dentin defects classified as type II dentin dysplasia and types II and III dentinogenesis imperfecta are caused by mutations in DSPP (dentin sialophosphoprotein). Most reported disease‐causing DSPP mutations occur within the repetitive DPP (dentin phosphoprotein) coding sequence. We cha...
Autores principales: | Yang, Jie, Kawasaki, Kazuhiko, Lee, Moses, Reid, Bryan M., Nunez, Stephanie M., Choi, Murim, Seymen, Figen, Koruyucu, Mine, Kasimoglu, Yelda, Estrella‐Yuson, Ninna, Lin, Brent P. J., Simmer, James P., Hu, Jan C.‐C. |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4707025/ https://www.ncbi.nlm.nih.gov/pubmed/26788535 http://dx.doi.org/10.1002/mgg3.176 |
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