FIGURE

Fig. 2

ID

ZDB-FIG-251117-12

Publication

Erkut et al., 2025 - A cardiovascular, craniofacial, and neurodevelopmental disorder caused by loss-of-function variants in the eIF3 complex component genes EIF3A and EIF3B

Other Figures

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Fig. 2

Photographs of probands with de novo variants in EIF3B or EIF3A (A–C) Clinical images of proband #4, with a canonical acceptor splice site variant in EIF3B; (D–F) proband #9 with a loss-of-function variant in EIF3B; (G–H) proband #15, with a loss-of-function variant EIF3A; and (I and J) proband #18, with a loss-of-function variant in EIF3A.

Expression Data

Expression Detail

Antibody Labeling

Phenotype Data

Phenotype Detail

Acknowledgments

This image is the copyrighted work of the attributed author or publisher, and ZFIN has permission only to display this image to its users. Additional permissions should be obtained from the applicable author or publisher of the image. Full text @ Am. J. Hum. Genet.