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

Author:

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 et al.

Publication:

The American Journal of Human Genetics

Publisher:

Elsevier

Date:

2 November 2017

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