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Case report
Two novel mutations in the CLCNKB gene leading to classic Bartter syndrome presenting as syncope and hypertension in a 13-year-old boy

Authors

  1. Correspondence to Dr Cuong M Duong; minh.duong{at}unsw.edu.au
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Citation

Le BT, Duong CM, Nguyen TQ, et al
Two novel mutations in the CLCNKB gene leading to classic Bartter syndrome presenting as syncope and hypertension in a 13-year-old boy

Publication history

  • Accepted June 2, 2020
  • First published July 5, 2020.
Online issue publication 
July 05, 2020

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