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Induced ablation of Bmp1 and Tll1 produces osteogenesis imperfecta in mice
Osteogenesis imperfecta (OI), or brittle bone disease, is most often caused by dominant mutations in the collagen I genes COL1A1/COL1A2, whereas rarer recessive OI is often caused by mutations in genes encoding collagen I-interacting proteins. Recently, mutations in the gene for the proteinase bone...
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| Main Authors: | , , , , , , , , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Oxford University Press
2014
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4030766/ https://ncbi.nlm.nih.gov/pubmed/24419319 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/hmg/ddu013 |
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