Iranian Journal of Pediatrics

Published by: Kowsar

A Chinese Girl with Bartter Syndrome Type III due to a Novel Mutation and/or Single Nucleotide Polymorphisms (SNPs) in CLCNKB Gene

Xiumin Wang 1 , Zheng Shen 2 , Meichun Xu 3 , * , Junfen Fu 4 and Li Liang 5
Article information
  • Iranian Journal of Pediatrics: February 28, 2013, 23 (1); 89-94
  • Published Online: December 13, 2012
  • Article Type: Case Report
  • Received: June 17, 2011
  • Accepted: April 01, 2012

To Cite: Wang X, Shen Z, Xu M, Fu J, Liang L. et al. A Chinese Girl with Bartter Syndrome Type III due to a Novel Mutation and/or Single Nucleotide Polymorphisms (SNPs) in CLCNKB Gene, Iran J Pediatr. 2013 ; 23(1):89-94.

Abstract
© 0, Author(s). This is an open-access article distributed under the terms of the Creative Commons Attribution-NonCommercial 4.0 International License (http://creativecommons.org/licenses/by-nc/4.0/) which permits copy and redistribute the material just in noncommercial usages, provided the original work is properly cited.
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Creative Commons License Except where otherwise noted, this work is licensed under Creative Commons Attribution Non Commercial 4.0 International License .

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