Innovative Journal of Pediatrics
The Scientific Journal of Growth & Development Research Center
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A Chinese Girl with Bartter Syndrome Type III due to a Novel Mutation and/or Single Nucleotide Polymorphisms (SNPs) in CLCNKB Gene
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Published online:Dec 13, 2012
Article type:Case Report
Received:Jun 17, 2011
Accepted:Apr 01, 2012
How to Cite:Wang X, Shen Z, Xu M, Fu J, Liang L. A Chinese Girl with Bartter Syndrome Type III due to a Novel Mutation and/or Single Nucleotide Polymorphisms (SNPs) in CLCNKB Gene. Inn J Pediatr. 2013;23(1):. doi:
Abstract
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© 2013, Author(s). This open-access article is available under the Creative Commons Attribution 4.0 (CC BY 4.0) International License (https://creativecommons.org/licenses/by/4.0/), which allows for unrestricted use, distribution, and reproduction in any medium, provided that the original work is properly cited.
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