Dentin dysplasia type I—A dental disease with genetic heterogeneity

Hereditary dentin disorders include dentinogenesis imperfecta (DGI) and dentin dysplasia (DD), which are autosomal dominant diseases characterized by altered dentin structure such as abnormality in dentin mineralization and the absence of root dentin. Shields classified DGI into three subgroups and...

Descripción completa

Detalles Bibliográficos
Autores principales: Chen, D, Li, X, Lu, F, Wang, Y, Xiong, F, Li, Q
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2018
Materias:
Review Articles
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7818184/
https://www.ncbi.nlm.nih.gov/pubmed/29575674
http://dx.doi.org/10.1111/odi.12861

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7818184/
https://www.ncbi.nlm.nih.gov/pubmed/29575674
http://dx.doi.org/10.1111/odi.12861

Ejemplares similares