Exome-wide Association Study Identifies GREB1L Mutations in Congenital Kidney Malformations
Sanna-Cherchi, Simone, Khan, Kamal, Westland, Rik, Krithivasan, Priya, Fievet, Lorraine, Rasouly, Hila Milo, Ionita-Laza, Iuliana, Capone, Valentina P., Fasel, David A., Kiryluk, Krzysztof, KamalakaraVolume:
101
Language:
english
Journal:
The American Journal of Human Genetics
DOI:
10.1016/j.ajhg.2017.09.018
Date:
November, 2017
File:
PDF, 1.06 MB
english, 2017