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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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Gorde:
Xehetasun bibliografikoak
Argitaratua izan da:J Endocr Soc
Egile Nagusiak: Alyusuf, Ebtihal Y, Ekhzaimy, Aishah A, Alzahrani, Ali
Formatua: Artigo
Hizkuntza:Inglês
Argitaratua: Oxford University Press 2021
Gaiak:
Sarrera elektronikoa: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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