Clinical and Genetic Features in 31 Serial Chinese Children With Gitelman Syndrome
Gitelman syndrome (GS, OMIM 263800) is a genetic congenital tubulopathy associated with salt loss, which is characterized by hypokalemic metabolic toxicity, hypocalciuria, and hypomagnesemia. GS, which is typically detected in adolescence or adulthood, has long been considered a benign tubular lesio...
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2021-04-01T00:00:00Z.
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