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Anatomical similarity between the Sost‐knockout mouse and sclerosteosis in humans
Sclerosteosis, a rare autosomal recessive genetic disorder caused by a mutation of the Sost gene, manifests in the facial skeleton by gigantism, facial distortion, mandibular prognathism, cranial nerve palsy, and, in extreme cases, compression of the medulla oblongata. Mice lacking sclerostin reflec...
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| Izdano u: | Anat Rec (Hoboken) |
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| Glavni autori: | , , , |
| Format: | Artigo |
| Jezik: | Inglês |
| Izdano: |
John Wiley & Sons, Inc.
2019
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| Teme: | |
| Online pristup: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7496997/ https://ncbi.nlm.nih.gov/pubmed/31729194 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/ar.24318 |
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