Exome-wide Association Study Identifies GREB1L Mutations in Congenital Kidney Malformations

S. Sanna-Cherchi, K. Khan, R. Westland, P. Krithivasan, L. Fievet, H.M. Rasouly, I. Ionita-Laza, V.P. Capone, D.A. Fasel, K. Kiryluk, S. Kamalakaran, M. Bodria, E.A. Otto, M.G. Sampson, C.E. Gillies, V. Vega-Warner, K. Vukojevic, I. Pediaditakis, G.S. Makar, A. MitrottiM. Verbitsky, J. Martino, Q. Liu, Y.-J. Na, V. Goj, G. Ardissino, M. Gigante, L. Gesualdo, M. Janezcko, M. Zaniew, C.L. Mendelsohn, S. Shril, F. Hildebrandt, J.A.E. van Wijk, A. Arapovic, M. Saraga, L. Allegri, C. Izzi, F. Scolari, V. Tasic, G.M. Ghiggeri, A. Latos-Bielenska, A.-M. Kiryluk, S. Mane, D.B. Goldstein, R.P. Lifton, N. Katsanis, E.E. Davis, A.G. Gharavi

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