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Cited by in F6Publishing
For: Yang W, Zhao S, Xie Y, Mo Z. A novel SLC12A3 homozygous c2039delG mutation in Gitelman syndrome with hypocalcemia. BMC Nephrol. 2018;19:362. [PMID: 30558554 DOI: 10.1186/s12882-018-1163-3] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 0.3] [Reference Citation Analysis]
Number Citing Articles
1 Chen SY, Jie N. Gitelman syndrome: A case report. World J Clin Cases 2022; 10(17): 5893-5898 [DOI: 10.12998/wjcc.v10.i17.5893] [Reference Citation Analysis]
2 De Silva N, Pathmanathan S, Sumanatilleke M, Dematapitiya C, Dissanayake P, Wijenayake U, Subasinghe V, Dissanayake V. A novel mutation of SLC12A3 gene causing Gitelman syndrome. SAGE Open Medical Case Reports 2022;10:2050313X2211022. [DOI: 10.1177/2050313x221102294] [Reference Citation Analysis]
3 Wang C. Novel heterozygous missense mutation of SLC12A3 gene in Gitelman syndrome: A case report. WJCC 2019;7:1522-8. [DOI: 10.12998/wjge.v7.i12.1522] [Cited by in CrossRef: 1] [Article Influence: 0.3] [Reference Citation Analysis]
4 Wang CL. Novel heterozygous missense mutation of SLC12A3 gene in Gitelman syndrome: A case report. World J Clin Cases 2019; 7(12): 1522-1528 [PMID: 31363482 DOI: 10.12998/wjcc.v7.i12.1522] [Cited by in F6Publishing: 1] [Reference Citation Analysis]