GitelmanSyndrome相关论文
人体细胞离子转运在维持细胞正常生理功能中起关键作用，溶质转运体(solute carrier，SLC)负责人体细胞大部分的离子转运。SLC12家族编......
Analysis of Mutations of Two Gitelman Syndrome Family SLC12A3 Genes and Proposed Treatments Using Ch
Objective:To determine the gene location of two Gitelman syndrome (GS) family SLC12A3 genes and explore treatments using......
Gitelman syndrome(GS)is a rare disease.Due to its diverse manifestations,it is often be misdiagnosed.We report A man wit......
目的探讨Gitelman综合征(Gitelman syndrome，GS)患儿基因型与骨代谢标志物、骨微结构的相关性。方法选择15例患儿作为GS组，并选择同......
Background Hereditary renal tubular disease can cause hypercalciuria,acid-base imbalance,hypokalemia,hypomagnesemia,rick......
