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Clinical Kidney Journal, ISSN 2048-8505, 06/2018, Volume 11, Issue 3, pp. 302 - 309
Journal Article
Nephrology Dialysis Transplantation, ISSN 0931-0509, 01/1992, Volume 7, Issue 9, pp. 896 - 901
Journal Article
Acta Paediatrica, ISSN 0803-5253, 01/2017, Volume 106, Issue 1, pp. 161 - 167
Aim Bartter syndrome is an autosomal‐recessive inherited disease in which patients present with hypokalaemia and metabolic alkalosis. We present two apparently... 
Bartter syndrome | Hypokalaemic alkalosis | SLC12A1 gene | Polyuria | HYPERCALCIURIA | ALKALOSIS | COTRANSPORTER | PEDIATRICS | MUTATIONS | Humans | Prenatal Diagnosis | Bartter Syndrome - diagnosis | Infant | Male | Genetic Markers | Mutation, Missense | Pregnancy | Solute Carrier Family 12, Member 1 - genetics | Homozygote | Bartter Syndrome - genetics | Pedigree | Female | Infant, Newborn | Family | Genes | Codon | Deoxyribonucleic acid--DNA
Journal Article
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