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Dental and Craniofacial Defects in the Crtap(−/−) Mouse Model of Osteogenesis Imperfecta Type VII
BACKGROUND: Inactivating mutations in the gene for cartilage-associated protein (CRTAP) cause osteogenesis imperfecta type VII in humans, with a phenotype that can include craniofacial defects. Dental and craniofacial manifestations have not been a focus of case reports to date. We analyzed the cran...
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| Publicado no: | Dev Dyn |
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| Main Authors: | , , , , , , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
2020
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7727892/ https://ncbi.nlm.nih.gov/pubmed/32133710 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/dvdy.166 |
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