[1]
Conticini, E. et al. 2020. Gitelman syndrome associated with chondrocalcinosis and severe neuropathy: a novel heterozygous mutation in SLC12A3 gene. Reumatismo. 72, 1 (Apr. 2020), 67–70. DOI:https://doi.org/10.4081/reumatismo.2020.1255.