Novel compound heterozygous mutation of SLC12A3 in Gitelman syndrome co-existent with hyperthyroidism: A case report and literature review

doi:10.12998/wjcc.v10.i21.7483

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Jul 26, 2022 (publication date) through Nov 4, 2024

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World Journal of Clinical Cases

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2307-8960

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

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World J Clin Cases. Jul 26, 2022; 10(21): 7483-7494
Published online Jul 26, 2022. doi: 10.12998/wjcc.v10.i21.7483

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Figure 1 Pedigree diagram showing proband (arrow) and segregation of SLC12A3.

Citation: Qin YZ, Liu YM, Wang Y, You C, Li LN, Zhou XY, Lv WM, Hong SH, Xiao LX. Novel compound heterozygous mutation of SLC12A3 in Gitelman syndrome co-existent with hyperthyroidism: A case report and literature review. World J Clin Cases 2022; 10(21): 7483-7494
URL: https://www.wjgnet.com/2307-8960/full/v10/i21/7483.htm
DOI: https://dx.doi.org/10.12998/wjcc.v10.i21.7483