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Recent progress in osteogenesis imperfecta
Osteogenesis imperfecta (OI), a rare clinical disease with abnormal type I collagen, is inherited or caused by mutation. A classification of OI into four types was proposed in 1979 and has been used up until four new types were added recently. A tough clinical challenge, OI causes abnormal blood coa...
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| Publicado no: | Orthop Surg |
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| Main Authors: | , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Blackwell Publishing Asia
2011
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6583639/ https://ncbi.nlm.nih.gov/pubmed/22009598 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1111/j.1757-7861.2011.00128.x |
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