FIGURE 6
- ID
- ZDB-FIG-211004-22
- Publication
- Xia et al., 2021 - A Dominant Heterozygous Mutation in COG4 Causes Saul-Wilson Syndrome, a Primordial Dwarfism, and Disrupts Zebrafish Development via Wnt Signaling
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LGK974 treatment suppresses shortened body length and chondrocyte defect caused by of |