1Berry MR, Robinson C, Karet Frankl FE.Unexpected clinical se- quelae of Gitelman syndrome : hypertension in adulthood is common and females have higher potassium requirements[J].Nephrol Dial Transplant,2013,28(6):1533-1542.
2Lii Q, Zhang Y, Song C, et al.A novel SLC12A3 gene homozygous mutation of Gitelman syndrome in an Asian pedigree and literature review[J].J Endocrinol Invest,2016,39(3):333-340.
3Luo J,Yang X,Liang J,et al.A pedigree analysis of two homozygous mutant Gitelman syndrome cases[J].Endocr J, 2015, 62(1):29-36.
4Tavira B,Gomez J,Santos F,et al.A labor- and cost-effective non- optical semiconductor (Ion Torrent)next-generation sequencing of the SLC12A3 and CLCNKA/B genes in Gitelman's syndrome pa- tients[J].J Hum Genet,2014,59(7):376-380.
5Koulouridis E, Koulouridis I.Molecular pathophysiology of Bartter's and Gitelman' s syndromes[J].World J Pediatr, 2015,11(2):113-125.
6Groenestege WM,Thebault S,van der Wijst J,et al.Impaired baso- lateral sorting of pro-EGF causes isolated recessive renal hypomag- nesemia[J].J Clin Invest,2007,117(8):2260-2267.
7Jiang L, Chen C, Yuan T, et al.Clinical severity of Gitelman syn- drome determined by serum magnesium impaired basolateral sort- ing of pro - EGF causes isolated recessive renal hypomagnesemia[J].Am J Nephrol,2014,39(4):357-366.
8Shao L, Ren H,Wang W, et al.Novel SLC12A3 mutations in Chi- nese patients with Gitelman, s syndrome[J].Nephron Physiol, 2008,108(3):29-36.
9Luo J,Yang X,Liang J,et al.A pedigree analysis of two homozygous mutant Gitelman syndrome cases[J].Endocr J, 2015, 62(1):29-36.
10Qin L, Shao L, Ren H, et al.Identification of five novel variants in the thiazide-sensitive NaCl co-transporter gene in Chinese patients with Gitelman syndrome[J].Nephrology (Carlton),2009,14( I):52-58.
