New SLC12A3 disease causative mutation of Gitelman&rsquo;s syndrome

doi:10.5527/wjn.v5.i6.551

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World Journal of Nephrology

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2220-6124

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Baishideng Publishing Group Inc, 7041 Koll Center Parkway, Suite 160, Pleasanton, CA 94566, USA

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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 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.

Citation: Grillone T, Menniti M, Bombardiere F, Vismara MFM, Belviso S, Fabiani F, Perrotti N, Iuliano R, Colao E. New SLC12A3 disease causative mutation of Gitelman’s syndrome. World J Nephrol 2016; 5(6): 551-555
URL: https://www.wjgnet.com/2220-6124/full/v5/i6/551.htm
DOI: https://dx.doi.org/10.5527/wjn.v5.i6.551

Grillone T, Menniti M, Bombardiere F, Vismara MFM, Belviso S, Fabiani F, Perrotti N, Iuliano R, Colao E. New SLC12A3 disease causative mutation of Gitelman’s syndrome. World J Nephrol 2016; 5(6): 551-555 [PMID: 27872838 DOI: 10.5527/wjn.v5.i6.551]

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