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Dental and craniofacial characteristics caused by the p.Ser40Leu mutation in IFITM5
Severe forms of osteogenesis imperfecta (OI) are usually caused by mutations in genes that code for collagen type I and frequently are associated with craniofacial abnormalities. However, the dental and craniofacial characteristics of OI caused by the p.Ser40Leu mutation in the IFITM5 gene have not...
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| Publicado no: | Am J Med Genet A |
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| Main Authors: | , , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
2018
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6347491/ https://ncbi.nlm.nih.gov/pubmed/30289614 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/ajmg.a.40383 |
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