A novel mutation in the chloride channel gene, CLCNKB, as a cause of Gitelman and Bartter syndromes
Author:
Publisher
Elsevier BV
Subject
Nephrology
Reference34 articles.
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4. A new familial disorder characterized by hypokalemia and hypomagnesaemia;Gitelman;Trans Assoc Am Physicians,1966
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3. Novel compound heterozygous variants of SLC12A3 gene in a Chinese patient with Gitelman syndrome: a case report;Frontiers in Genetics;2023-06-12
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