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...

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Detalles Bibliográficos
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.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2015
Materias:
Original Articles
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

Internet

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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