Gitelman syndrome associated with chondrocalcinosis and severe neuropathy: a novel heterozygous mutation in SLC12A3 gene. Reumatismo, [S. l.], v. 72, n. 1, p. 67–70, 2020. DOI: 10.4081/reumatismo.2020.1255. Disponível em: https://www.reumatismo.org/reuma/article/view/1255. Acesso em: 14 jun. 2025.