Deletion of sf3b4 causes splicing defects and gene dysregulation that disrupt craniofacial development and survival.
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PubMed
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| Main Authors: | , , , , , |
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| Format: | Artículo científico |
| Language: | en |
| Published: |
Disease models & mechanisms
2025
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| Subjects: | |
| Online Access: | |
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