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Dentinogenesis imperfecta type I: A case report with literature review on nomenclature system
Dentinogenesis imperfecta (DI) is an inherited disorder affecting dentin. Defective dentin formation results in discolored teeth that are prone to attrition and fracture. Mutation in dentin sialophosphoprotein (DSPP) has been found to cause the dentin disorders DI - I and II (shields II and III). Ea...
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| Main Authors: | , , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Medknow Publications & Media Pvt Ltd
2014
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4211222/ https://ncbi.nlm.nih.gov/pubmed/25364163 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.4103/0973-029X.141363 |
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