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A Novel Mutation in SOST Gene Causes Sclerosteosis
Background: Sclerostin is a SOST gene product that inhibits osteoblasts activity and prevents excessive bone formation by antagonizing Wnt signaling pathway. Sclerosteosis has been linked to the loss of function mutation in SOST gene. It is a rare autosomal recessive disorder characterized by cranio...
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| Publicat a: | J Endocr Soc |
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| Autors principals: | , , |
| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
Oxford University Press
2021
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| Matèries: | |
| Accés en línia: | https://ncbi.nlm.nih.gov/pmc/articles/PMC8089814/ https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1210/jendso/bvab048.358 |
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