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In Vivo Functional Study of Disease-associated Rare Human Variants Using Drosophila
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Neurodevelopmental trajectories and mis-splicing in Chinese patients caused by novel EFTUD2 mutations
Hua Xie1, Xiaoli Liu2, Pengfei Luan1
1Department of Medical Genetics, Capital Center for Children's Health, Capital Medical University, Capital Institute of Pediatrics, China.
Gene
|September 22, 2025
Abstract
No abstract available in PubMed .
Keywords:
Developmental trajectoryEFTUD2 geneMandibulofacial dysostosis with microcephalyMis-splicingMore Related Videos
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