Deletion of sf3b4 causes splicing defects and gene dysregulation that disrupt craniofacial development and survival.
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PubMed
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| Auteurs principaux: | Griffin, Casey, Coppenrath, Kelsey, Khan, Doha, Lin, Ziyan, Horb, Marko, Saint-Jeannet, Jean-Pierre |
|---|---|
| Format: | Artículo científico |
| Langue: | en |
| Publié: |
Disease models & mechanisms
2025
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