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Connective tissue alterations in Fkbp10(−/−) mice
Osteogenesis imperfecta (OI) is an inherited brittle bone disorder characterized by bone fragility and low bone mass. Loss of function mutations in FK506-binding protein 10 (FKBP10), encoding the FKBP65 protein, result in recessive OI and Bruck syndrome, of which the latter is additionally character...
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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/PMC4140464/ https://ncbi.nlm.nih.gov/pubmed/24777781 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/hmg/ddu197 |
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