For: | 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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URL: | https://www.wjgnet.com/2220-6124/full/v5/i6/551.htm |
Number | Citing Articles |
1 |
Rita Veríssimo, Luís Leite de Sousa, Tiago J Carvalho, Pedro Fidalgo. Novel SLC12A3 mutation in Gitelman syndrome. BMJ Case Reports 2021; 14(1): e238097 doi: 10.1136/bcr-2020-238097
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2 |
Verdiana Ravarotto, Giovanni Bertoldi, Lucia Federica Stefanelli, Laura Gobbi, Lorenzo A. Calò. Molecular aspects of the altered Angiotensin II signaling in Gitelman’s syndrome. Expert Opinion on Orphan Drugs 2022; 10(1): 1 doi: 10.1080/21678707.2022.2066996
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