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The swaying mouse as a model of osteogenesis imperfecta caused by WNT1 mutations
Osteogenesis imperfecta (OI) is a heritable disorder of connective tissue characterized by bone fragility and low bone mass. Recently, our group and others reported that WNT1 recessive mutations cause OI, whereas WNT1 heterozygous mutations cause early onset osteoporosis. These findings support the...
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| Glavni autori: | , , , , , , , , , |
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| Format: | Artigo |
| Jezik: | Inglês |
| Izdano: |
Oxford University Press
2014
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| Teme: | |
| Online pristup: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4082367/ https://ncbi.nlm.nih.gov/pubmed/24634143 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/hmg/ddu117 |
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