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