Exome-wide Association Study Identifies GREB1L Mutations in Congenital Kidney Malformations.
49 auth. S. Sanna-Cherchi, Kamal Khan, R. Westland, Priya Krithivasan, Lorraine Fievet, H. Rasouly, I. Ionita-Laza, Valentina Capone, D. Fasel, K. Kiryluk, S. Kamalakaran, M. Bodria, E. Otto, M. Sampson, C. Gillies, ... V. Vega-Warner, K. Vukojević, Igor Pediaditakis, Gabriel S. Makar, A. Mitrotti, M. Verbitsky, Jeremiah Martino, Qingxue Liu, Y. Na, V. Goj, G. Ardissino, M. Gigante, L. Gesualdo, M. Janezcko, M. Zaniew, C. Mendelsohn, S. Shril, F. Hildebrandt, J. V. van Wijk, Adela Arapović, M. Saraga, L. Allegri, C. Izzi, F. Scolari, V. Tasic, G. Ghiggeri, A. Latos-Bieleńska, A. Materna-Kiryluk, S. Mane, D. Goldstein, R. Lifton, N. Katsanis, E. Davis, A. Gharavi