Condition: RENAL HYPODYSPLASIA/APLASIA 3
rs1409376788
in
GREB1L
gene and
RENAL HYPODYSPLASIA/APLASIA 3
PMID 29100091
2017 Mutations in GREB1L Cause Bilateral Kidney Agenesis in Humans and Mice.
PMID 29100090
2017 Exome-wide Association Study Identifies GREB1L Mutations in Congenital Kidney Malformations.
PMID 28739660
2017 A Gene Implicated in Activation of Retinoic Acid Receptor Targets Is a Novel Renal Agenesis Gene in Humans.