Exome-wide Association Study Identifies GREB1L Mutations in Congenital Kidney Malformations
(The American Journal of Human Genetics 101, 789 –802; November 2, 2017)
Source: The American Journal of Human Genetics - Category: Genetics & Stem Cells Authors: Simone Sanna-Cherchi, Kamal Khan, Rik Westland, Priya Krithivasan, Lorraine Fievet, Hila Milo Rasouly, Iuliana Ionita-Laza, Valentina P. Capone, David A. Fasel, Krzysztof Kiryluk, Sitharthan Kamalakaran, Monica Bodria, Edgar A. Otto, Matthew G. Sampson, C Tags: Correction Source Type: research