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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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| Publicat a: | Mol Genet Genomic Med |
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| Autors principals: | , , , , |
| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
John Wiley and Sons Inc.
2018
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| Matèries: | |
| Accés en línia: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6014476/ https://ncbi.nlm.nih.gov/pubmed/29512331 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/mgg3.375 |
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