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March 14, 2014Human Molecular GeneticsOpen Access

The swaying mouse as a model of osteogenesis imperfecta caused by WNT1 mutations

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Authors

KJKyu Sang JoengYLYi-Chien LeeMJMing-Ming Jiang

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Joeng et al. (2014) studied this question.

synapsesocial.com/papers/6aa4fa2dc19a1092ac812535https://doi.org/10.1093/hmg/ddu117
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  1. 1<i>CRTAP</i>and<i>LEPRE1</i>mutations in recessive osteogenesis imperfecta2008 · 209 citations
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  3. 3Sclerostin Mediates Bone Response to Mechanical Unloading Through Antagonizing Wnt/β-Catenin Signaling2009 · 630 citations
  4. 4Mutations in WNT1 are a cause of osteogenesis imperfecta2013 · 197 citations