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Sep 26, 2020 (publication date) through Jun 9, 2024
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Publication Name
World Journal of Clinical Cases
ISSN
2307-8960
Publisher of This Article
Baishideng Publishing Group Inc, 7041 Koll Center Parkway, Suite 160, Pleasanton, CA 94566, USA
| For: | Yu RZ, Chen MS. Gitelman syndrome caused by a rare homozygous mutation in the SLC12A3 gene: A case report. World J Clin Cases 2020; 8(18): 4252-4258 [PMID: 33024786 DOI: 10.12998/wjcc.v8.i18.4252] |
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| URL: | https://www.wjgnet.com/2307-8960/full/v8/i18/4252.htm |
| Number | Citing Articles |
| 1 |
Melis Akpinar Gozetici, Fadime Ersoy Dursun, Hasan Dursun. Three uncommon mutations of the SLC12A3 gene in gitelman syndrome: case reports and review of the literature. Egyptian Journal of Medical Human Genetics 2022; 23(1) doi: 10.1186/s43042-022-00288-8
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| 2 |
Neomal De Silva, Sivatharshya Pathmanathan, Manilka Sumanatilleke, Chinthana Dematapitiya, Preethi Dissanayake, Umesha Wijenayake, Vindya Subasinghe, Vajira Dissanayake. A novel mutation of SLC12A3 gene causing Gitelman syndrome. SAGE Open Medical Case Reports 2022; 10: 2050313X2211022 doi: 10.1177/2050313X221102294
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