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A new syndrome. Am J Med 33: 811\u2013828.","DOI":"10.1016\/0002-9343(62)90214-0"},{"key":"2","doi-asserted-by":"crossref","unstructured":"2 Simon DB, Karet FE, Hamdan JM, DiPietro A, Sanjad SA, et al. (1996) Bartter\u2019s syndrome, hypokalaemic alkalosis with hypercalciuria, is caused by mutations in the Na-K-2Cl cotransporter NKCC2. Nat Genet 13: 183\u2013188.","DOI":"10.1038\/ng0696-183"},{"key":"3","doi-asserted-by":"crossref","unstructured":"3 Simon DB, Karet FE, Rodriguez-Soriano J, Hamdan JH, DiPietro A, et al. (1996) Genetic heterogeneity of Bartter\u2019s syndrome revealed by mutations in the K+ channel, ROMK. Nat Genet 14: 152\u2013156.","DOI":"10.1038\/ng1096-152"},{"key":"4","doi-asserted-by":"crossref","unstructured":"4 Simon DB, Bindra RS, Mansfield TA, Nelson-Williams C, Mendonca E, et al. (1997) Mutations in the chloride channel gene, CLCNKB, cause Bartter\u2019s syndrome type III. Nat Genet 17: 171\u2013178.","DOI":"10.1038\/ng1097-171"},{"key":"5","doi-asserted-by":"crossref","unstructured":"5 Birkenh\u00e4ger R, Otto E, Sch\u00fcrmann MJ, Vollmer M, Ruf EM, et al. (2001) Mutation of BSND causes Bartter syndrome with sensorineural deafness and kidney failure. Nat Genet 29: 310\u2013314.","DOI":"10.1038\/ng752"},{"key":"6","doi-asserted-by":"crossref","unstructured":"6 Schlingmann KP, Konrad M, Jeck N, Waldegger P, Reinalter SC, et al. (2004) Salt wasting and deafness resulting from mutations in two chloride channels. N Engl J Med 350: 1314\u20131319.","DOI":"10.1056\/NEJMoa032843"},{"key":"7","doi-asserted-by":"crossref","unstructured":"7 Laghmani K, Beck BB, Yang SS, Seaayfan E, Wenzel A, et al. (2016) Polyhydramnios, transient antenatal Bartter\u2019s Syndrome, and MAGED2 mutations. N Engl J Med 374: 1853\u20131863.","DOI":"10.1056\/NEJMoa1507629"},{"key":"8","doi-asserted-by":"crossref","unstructured":"8 Tajima T, Nawate M, Takahashi Y, Mizoguchi Y, Sugihara S, et al. (2006) Molecular analysis of the CLCNKB gene in Japanese patients with classic Bartter syndrome. Endocr J 53: 647\u2013652.","DOI":"10.1507\/endocrj.K06-034"},{"key":"9","doi-asserted-by":"crossref","unstructured":"9 Seys E, Andrini O, Keck M, Mansour-Hendili L, Courand PY, et al. (2017) Clinical and genetic spectrum of Bartter Syndrome type 3. J Am Soc Nephrol 28: 2540\u20132552.","DOI":"10.1681\/ASN.2016101057"},{"key":"10","unstructured":"10 Yu Y, Pan X, Ren H, Wang W, Chen N (2010) Study on CLCNKB gene mutation in a late-onset Chinese patient with classic Bartter syndrome. Chin Journal Nephrol 26: 598\u2013602."},{"key":"11","unstructured":"11 Feng C, Zhang H, Chen Y, Chen X (2021) A case of Adult Classic Bartter syndrome caused by a new compound heterozygous mutation in CLCNKB gene. New Clinical Medicine in China 14: 925\u2013928 (In Chinese)."},{"key":"12","doi-asserted-by":"crossref","unstructured":"12 Tamagawa E, Inaba H, Ota T, Ariyasu H, Kawashima H, et al. (2014) Bartter syndrome type 3 in an elderly complicated with adrenocorticotropin-deficiency. Endocr J 61: 855\u2013860.","DOI":"10.1507\/endocrj.EJ14-0125"},{"key":"13","unstructured":"13 Huang Q, Yang C, Li S, Su Y, Zeng L (2015) Approach to the patient with typical Bartter\u2019s syndrome and metabolic syndrome: diagnosis and treatment. Chin J Endocrinol Metab 31: 169\u2013171 (In Chinese)."},{"key":"14","doi-asserted-by":"crossref","unstructured":"14 Colussi G, De Ferrari ME, Tedeschi S, Prandoni S, Syr\u00e9n ML, et al. (2002) Bartter syndrome type 3: an unusual cause of nephrolithiasis. Nephrol Dial Transplant 17: 521\u2013523.","DOI":"10.1093\/ndt\/17.3.521"},{"key":"15","doi-asserted-by":"crossref","unstructured":"15 Xue Y, Wang B, Tang R, Ni H, Chen P, et al. (2019) Bartter syndrome type III with only a synonymous mutation of the CLCNKB gene. Clin Nephrol 92: 325\u2013328.","DOI":"10.5414\/CN109784"},{"key":"16","doi-asserted-by":"crossref","unstructured":"16 Lee JW, Lee J, Heo NJ, Cheong HI, Han JS (2016) Mutations in SLC12A3 and CLCNKB and their correlation with clinical phenotype in patients with Gitelman and Gitelman-like syndrome. J Korean Med Sci 31: 47\u201354.","DOI":"10.3346\/jkms.2016.31.1.47"},{"key":"17","doi-asserted-by":"crossref","unstructured":"17 Chiang WF, Lin SH, Chan JS, Lin SH (2014) Hypokalemic paralysis in a middle-aged female with classic Bartter syndrome. Clin Nephrol 81: 146\u2013150.","DOI":"10.5414\/CN107606"},{"key":"18","doi-asserted-by":"crossref","unstructured":"18 Qasba RK, Bucharles A, Piccoli M, Sharma P, Banga A, et al. (2023) Bartter syndrome: a systematic review of case reports and case series. Medicina (Kaunas) 59: 1638.","DOI":"10.3390\/medicina59091638"},{"key":"19","doi-asserted-by":"crossref","unstructured":"19 Han Y, Cheng H, Shao S, Lang Y, Zhao X, et al. (2020) Thirteen novel CLCNKB variants and genotype\/phenotype association study in 42 Chinese patients with Bartter syndrome type 3. Endocrine 68: 192\u2013202.","DOI":"10.1007\/s12020-019-02156-9"},{"key":"20","doi-asserted-by":"crossref","unstructured":"20 Konrad M, Nijenhuis T, Ariceta G, Bertholet-Thomas A, Calo LA, et al. (2021) Diagnosis and management of Bartter syndrome: executive summary of the consensus and recommendations from the European Rare Kidney Disease Reference Network Working Group for Tubular Disorders. Kidney Int 99: 324\u2013335.","DOI":"10.1016\/j.kint.2020.10.035"},{"key":"21","doi-asserted-by":"crossref","unstructured":"21 Han Y, Lin Y, Sun Q, Wang S, Gao Y, et al. (2017) Mutation spectrum of Chinese patients with Bartter syndrome. Oncotarget 8: 101614\u2013101622.","DOI":"10.18632\/oncotarget.21355"},{"key":"22","doi-asserted-by":"crossref","unstructured":"22 Ren H, Qin L, Wang W, Ma J, Zhang W, et al. (2013) Abnormal glucose metabolism and insulin sensitivity in Chinese patients with Gitelman syndrome. Am J Nephrol 37: 152\u2013157.","DOI":"10.1159\/000346708"},{"key":"23","doi-asserted-by":"crossref","unstructured":"23 Liu T, Wang C, Lu J, Zhao X, Lang Y, et al. (2016) Genotype\/phenotype analysis in 67 Chinese patients with Gitelman\u2019s Syndrome. Am J Nephrol 44: 159\u2013168.","DOI":"10.1159\/000448694"},{"key":"24","doi-asserted-by":"crossref","unstructured":"24 Yuan T, Jiang L, Chen C, Peng X, Nie M, et al. (2017) Glucose tolerance and insulin responsiveness in Gitelman syndrome patients. Endocr Connect 6: 243\u2013252.","DOI":"10.1530\/EC-17-0014"},{"key":"25","doi-asserted-by":"crossref","unstructured":"25 Knoers NV, Levtchenko EN (2008) Gitelman syndrome. 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