Xla Wt + ctnnb1 MO has 1 phenotype(s)
Images Sources Experiment + Assay Phenotypes Human Diseases
Fig. J

Kreis J et al. (2021)
Xla Wt + ctnnb1 MO

NF10-11.5 (in situ hybridization)
Expression Phenotype
absent myod1.L expression in ventral marginal zone