- Title
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De novo truncating variant in the FBRSL1 gene caused neurodevelopmental disorders, epilepsy, congenital heart disease, and facial dysmorphism
- Authors
- Xu, D., Zhang, X.L., Wang, P.Y., Chu, M.M., Xie, J.Y., Wang, M.Y., Li, X.L., Xu, Y.F., Liu, J., Wen, Q.R., Fang, Y., Gao, J.S., Xu, F.L., Luo, S.
- Source
- Full text @ Exp. Neurol.
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ZFIN is incorporating published figure images and captions as part of an ongoing project. Figures from some publications have not yet been curated, or are not available for display because of copyright restrictions. |