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Original Article
PBX1 haploinsufficiency leads to syndromic congenital anomalies of the kidney and urinary tract (CAKUT) in humans
- Correspondence to Dr Charles Coutton, Département de Génétique et Procréation, CHU Grenoble Alpes, Grenoble, France; CCoutton{at}chu-grenoble.fr
Citation
PBX1 haploinsufficiency leads to syndromic congenital anomalies of the kidney and urinary tract (CAKUT) in humans
Publication history
- Received November 7, 2016
- Revised January 3, 2017
- Accepted January 17, 2017
- First published March 7, 2017.
Online issue publication
June 21, 2017
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- Previous version (7 March 2017).
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© Article author(s) (or their employer(s) unless otherwise stated in the text of the article) 2017. All rights reserved. No commercial use is permitted unless otherwise expressly granted.