Title : [Establishment of genetic testing for Gitelman's syndrome].

Pub. Date : 2010 Feb

PMID : 20229814






1 Functional Relationships(s)
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1 Gitelman"s syndrome is an autosomal recessive disorder marked by salt wasting and hypokalaemia resulting from loss of-function mutations in the SLC12A3 gene that codes for the thiazide sensitive Na -Cl cotransporter. Salts solute carrier family 12 member 3 Homo sapiens