e-Article
Exome-wide Association Study Identifies GREB1L Mutations in Congenital Kidney Malformations
Document Type
Article
Author
Sanna-Cherchi, S.; Westland, R.; Krithivasan, P.; Rasouly, H.M.; Capone, V.P.; Fasel, D.A.; Kiryluk, K.; Makar, G.S.; Mitrotti, A.; Verbitsky, M.; Martino, J.; Liu, Q.; Na, Y.-J.; Gharavi, A.G.; Khan, K.; Fievet, L.; Pediaditakis, I.; Katsanis, N.; Davis, E.E.; van Wijk, J.A.E.; Ionita-Laza, I.; Kamalakaran, S.; Goldstein, D.B.; Bodria, M.; Ghiggeri, G.M.; Otto, E.A.; Sampson, M.G.; Gillies, C.E.; Vega-Warner, V.; Vukojevic, K.; Goj, V.; Ardissino, G.; Gigante, M.; Gesualdo, L.; Janezcko, M.; Zaniew, M.; Mendelsohn, C.L.; Shril, S.; Hildebrandt, F.; Arapovic, A.; Saraga, M.; Allegri, L.; Izzi, C.; Scolari, F.; Tasic, V.; Latos-Bielenska, A.; Materna-Kiryluk, A.; Mane, S.; Lifton, R.P.
Source
In: American Journal of Human Genetics . (American Journal of Human Genetics, 2 November 2017, 101(5):789-802)
Subject
Language
English
ISSN
15376605
00029297
00029297