Associated Papers
Clinical, genetic characteristics and outcome of four Chinese patients with Bartter syndrome type 3: Further insight into a genotype-phenotype correlation.
Piao Y et al.
Molecular Genetics and Metabolism Reports, 2024
[Gitelman´s syndrome as common cause of hypokalemia and hypomagnesemia].
Ryšavá R et al.
Vnitrni Lekarstvi, 2016
DNA analysis of renal electrolyte transporter genes among patients suffering from Bartter and Gitelman syndromes: summary of mutation screening.
Urbanová M et al.
Folia Biologica, 2011
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