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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Váldodahkkit: Lingxia Zhang (Dahkki), Ke Huang (Dahkki), Shugang Wang (Dahkki), Haidong Fu (Dahkki), Jingjing Wang (Dahkki), Huijun Shen (Dahkki), Zhihong Lu (Dahkki), Junyi Chen (Dahkki), Yu Bao (Dahkki), Chunyue Feng (Dahkki), Guanping Dong (Dahkki), Jianhua Mao (Dahkki)
Materiálatiipa: Girji
Almmustuhtton: Frontiers Media S.A., 2021-04-01T00:00:00Z.
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3rd Floor Main Library

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