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Severe Osteogenesis Imperfecta in Cyclophilin B–Deficient Mice
Osteogenesis Imperfecta (OI) is a human syndrome characterized by exquisitely fragile bones due to osteoporosis. The majority of autosomal dominant OI cases result from point or splice site mutations in the type I collagen genes, which are thought to lead to aberrant osteoid within developing bones....
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| Main Authors: | , , , , , , , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Public Library of Science
2009
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC2777385/ https://ncbi.nlm.nih.gov/pubmed/19997487 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1371/journal.pgen.1000750 |
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