Sanna-Cherchi et al., 2017
- Exome-wide Association Study Identifies GREB1L Mutations in Congenital Kidney Malformations.
American journal of human genetics
101:789-802
Full text @ Am. J. Hum. Genet.
Human Disease | Fish | Environment | Evidence Code |
---|---|---|---|
CAKUT | |||
renal agenesis |
EKW + MO2-greb1l greb1lrdu1000/rdu1000 |
standard conditions standard conditions |
|