Dentinogenesis imperfecta type II‐ genotype and phenotype analyses in three Danish families

BACKGROUND: Dentinogenesis imperfecta (DI) is a rare debilitating hereditary disorder affecting dentin formation and causing loss of the overlying enamel. Clinically, DI sufferers have a discolored and weakened dentition with an increased risk of fracture. The aims of this study were to assess genot...

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Detalles Bibliográficos
Autores principales: Taleb, Kawther, Lauridsen, Eva, Daugaard‐Jensen, Jette, Nieminen, Pekka, Kreiborg, Sven
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2018
Materias:
Original Articles
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6014476/
https://www.ncbi.nlm.nih.gov/pubmed/29512331
http://dx.doi.org/10.1002/mgg3.375

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6014476/
https://www.ncbi.nlm.nih.gov/pubmed/29512331
http://dx.doi.org/10.1002/mgg3.375

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