Exome-wide Association Study Identifies GREB1L Mutations in Congenital Kidney MalformationsSimone Sanna‐Cherchi, Ali G. Gharavi, Kamal Khan et al.|The American Journal of Human Genetics|2017Cited by 106
Loss of Zeb2 in mesenchyme-derived nephrons causes primary glomerulocystic diseaseHila Milo Rasouly, Lu W, Richa Sharma et al.|Kidney International|2016Cited by 21