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Activation of WNT signaling restores the facial deficits in a zebrafish with defects in cholesterol metabolism
Inborn errors of cholesterol metabolism occur as a result of mutations in the cholesterol synthesis pathway (CSP). Although mutations in the CSP cause a multiple congenital anomaly syndrome, craniofacial abnormalities are a hallmark phenotype associated with these disorders. Previous studies have es...
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| 出版年: | Genesis |
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| 主要な著者: | , , , , , |
| フォーマット: | Artigo |
| 言語: | Inglês |
| 出版事項: |
John Wiley & Sons, Inc.
2020
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| 主題: | |
| オンライン･アクセス: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7816230/ https://ncbi.nlm.nih.gov/pubmed/33197123 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/dvg.23397 |
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