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Non-Syndromic Dentinogenesis Imperfecta Caused by Mild Mutations in COL1A2
Hereditary dentin defects can be categorized as a syndromic form predominantly related to osteogenesis imperfecta (OI) or isolated forms without other non-oral phenotypes. Mutations in the gene encoding dentin sialophosphoprotein (DSPP) have been identified to cause dentinogenesis imperfecta (DGI) T...
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| Publicado no: | J Pers Med |
|---|---|
| Main Authors: | , , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
MDPI
2021
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC8229930/ https://ncbi.nlm.nih.gov/pubmed/34201399 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3390/jpm11060526 |
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