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Recent developments in osteogenesis imperfecta
Osteogenesis imperfecta (OI) is an uncommon genetic bone disease associated with brittle bones and fractures in children and adults. Although OI is most commonly associated with mutations of the genes for type I collagen, many other genes (some associated with type I collagen processing) have now be...
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| Publicado no: | F1000Res |
|---|---|
| Main Authors: | , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
F1000Research
2015
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4566283/ https://ncbi.nlm.nih.gov/pubmed/26401268 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.12688/f1000research.6398.1 |
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