Title : Gitelman syndrome with normocalciuria - a case report.

Pub. Date : 2022 May 4

PMID : 35509038






2 Functional Relationships(s)
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Protein Name
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1 BACKGROUND: Gitelman Syndrome (GS) is a hereditary tubulopathy associated with a biallelic inactivating mutations of the SLC12A3 gene encoding the thiazide-sensitive sodium-chloride cotransporter (NCCT). Chlorides solute carrier family 12 member 3 Homo sapiens
2 BACKGROUND: Gitelman Syndrome (GS) is a hereditary tubulopathy associated with a biallelic inactivating mutations of the SLC12A3 gene encoding the thiazide-sensitive sodium-chloride cotransporter (NCCT). Chlorides solute carrier family 12 member 3 Homo sapiens