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Original Article
PBX1 haploinsufficiency leads to syndromic congenital anomalies of the kidney and urinary tract (CAKUT) in humans

Authors

  1. Correspondence to Dr Charles Coutton, Département de Génétique et Procréation, CHU Grenoble Alpes, Grenoble, France; CCoutton{at}chu-grenoble.fr
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Citation

Le Tanno P, Breton J, Bidart M, et al
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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