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AB107. Study of functional independence of patients with osteogenesis imperfecta
BACKGROUND: Osteogenesis imperfecta (OI) is a genetic bone disorder characterized by fragile bones that break easily. It is a complicated, variable and rare disorder. Its major feature is a fragile skeleton, but many other body systems are also affected. OI is caused by a mutation in a gene that aff...
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| Udgivet i: | Ann Transl Med |
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| Main Authors: | , , , , , , , |
| Format: | Artigo |
| Sprog: | Inglês |
| Udgivet: |
AME Publishing Company
2017
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| Fag: | |
| Online adgang: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5641763/ https://ncbi.nlm.nih.govhttp://dx.doi.org/10.21037/atm.2017.s107 |
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