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• W3048496994 abstract "Patients with Gitelman syndrome present with an inherited salt-losing tubulopathy induced by loss-of-function mutations in the SLC12A3 gene encoding the apically expressed thiazide-sensitive NaCl cotransporter of the distal convoluted tubule. Patients usually have electrolyte disorders, including" @default.
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• W3048496994 date "2020-08-12" @default.
• W3048496994 modified "2023-10-02" @default.
• W3048496994 title "QT Interval in Adult with Chronic Hypokalemia due to Gitelman Syndrome" @default.
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• W3048496994 doi "https://doi.org/10.2215/cjn.07540520" @default.
• W3048496994 hasPubMedCentralId "https://www.ncbi.nlm.nih.gov/pmc/articles/7646245" @default.
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