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Rdh10 loss-of-function and perturbed retinoid signaling underlies the etiology of choanal atresia
Craniofacial development is a complex process that involves sequential growth and fusion of the facial prominences. When these processes fail, congenital craniofacial anomalies can occur. For example, choanal atresia (CA) is a congenital craniofacial anomaly in which the connection between the nasal...
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| Publicado no: | Hum Mol Genet |
|---|---|
| Main Authors: | , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Oxford University Press
2017
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5390677/ https://ncbi.nlm.nih.gov/pubmed/28169399 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/hmg/ddx031 |
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