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Cited by in CrossRef
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]
URL: https://www.wjgnet.com/2307-8960/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 syndromeBMJ Case Reports 2021; 14(1): e238097 doi: 10.1136/bcr-2020-238097
2
Verdiana Ravarotto, Giovanni Bertoldi, Lucia Federica Stefanelli, Laura Gobbi, Lorenzo A. Calò. Molecular aspects of the altered Angiotensin II signaling in Gitelman’s syndromeExpert Opinion on Orphan Drugs 2022; 10(1): 1 doi: 10.1080/21678707.2022.2066996