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Cited by in CrossRef
For: 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 [PMID: 36158002 DOI: 10.12998/wjcc.v10.i21.7483]
URL: https://www.wjgnet.com/2307-8960/full/v10/i21/7483.htm
Number Citing Articles
1
Oguzhan Koca, Mustafa Tarık Alay, Ahmet Murt, Aysel Kalayci Yigin, Mehmet Seven, Isil Bavunoglu. A novel homozygous SLC12A3 mutation causing Gitelman syndrome with co-existent autoimmune thyroiditis: a case report and review of the literatureCEN Case Reports 2024;  doi: 10.1007/s13730-023-00845-z