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 / Model Data (2 Records)
Human Disease Fish Environment Evidence Code
CAKUT
renal agenesis EKW + MO2-greb1l
greb1lrdu1000/rdu1000
standard conditions
standard conditions