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| A novel mutation of |
| Hee-Won Cho, Sang Taek Lee, Heeyeon Cho, Hae Il Cheong |
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Clin Exp Pediatr. 2016;59(Suppl 1):S103-S106. Published online November 30, 2016 DOI: https://doi.org/10.3345/kjp.2016.59.11.S103 |
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A novel mutation ofCLCNKBin a Korean patient of mixed phenotype of Bartter-Gitelman syndrome Korean Journal of Pediatrics. 2016;59(Suppl 1):S103  Mixed Bartter-Gitelman syndrome: an inbred family with a heterogeneous phenotype expression of a novel variant in the CLCNKB gene SpringerPlus. 2014;3(1): Erratum: Mutations in SLC12A3 and CLCNKB and Their Correlation with Clinical Phenotype in Patients with Gitelman and Gitelman-like Syndrome Journal of Korean Medical Science. 2016;31(5):827 A novel mutation in the chloride channel gene, CLCNKB, as a cause of Gitelman and Bartter syndromes Kidney International. 2003;63(1):24-32 A novel mutation of CLCNKB in a Japanese patient of Gitelman-like phenotype with diuretic insensitivity to thiazide administration Meta Gene. 2014;2:342-348 Bartter syndrome and Gitelman syndrome Korean Journal of Electrolyte Metabolism. 2004;2(1):13 Bartter syndrome and growth hormone deficiency: Three siblings with a novel CLCNKB
mutation Pediatrics International. 2019;61(2):193-197 A Patient with Irritable Bowel Syndrome Improved After Treatment with <italic>Sosiho-tang</italic>, <italic>Jakyakgamcho-tang</italic>, and Acupuncture: A Case Report The Journal of Internal Korean Medicine. 2022;43(5):960-966 NovelCLCNKBMutations Causing Bartter Syndrome Affect Channel Surface Expression Human Mutation. 2013;34(9):1269-1278 Bartter syndrome in two sisters with a novel mutation of the CLCNKB gene, one with deafness European Journal of Pediatrics. 2011;170(9):1209-1211 |
