换一批摘要Hypokalemia is among the most common electrolyte disorders in clinical practice and severe condition is life-threatening and has received extensive attention in clinical practice.Genetic diagnosis remains the gold standard for the diagnosis and identification of hereditary renal tubular diseases.Below is the report of genotyping and diagnosis of a case of secondary Gitelman syndrome (GS) based on next-generation sequencing.
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DOI
10.4103/0366-6999.176992
发布时间
2016-04-07（万方平台首次上网日期，不代表论文的发表时间）
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