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Nov 6, 2016 (publication date) through May 20, 2026
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World Journal of Nephrology
ISSN
2220-6124
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Baishideng Publishing Group Inc, 7041 Koll Center Parkway, Suite 160, Pleasanton, CA 94566, USA

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©The Author(s) 2016.
World J Nephrol. Nov 6, 2016; 5(6): 551-555
Published online Nov 6, 2016. doi: 10.5527/wjn.v5.i6.551
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Figure 1 Electropherograms showing DNA sequences of exon 2 (A), exon 22 (B) and exon 23 (C), in the regions containing the variations detected.
Figure 2
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Figure 2 Pedigree of family. Gitelman’s syndrome affected patients are colored in black, heterozygous carriers are filled in gray. Mutations and polymorphisms of subjects are reported close to their respective symbols.
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