Magnesium

solute carrier family 12 member 3 ; Homo sapiens







6 Article(s)
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PMID
Title
Pub. Year
#Total Relationships
1 33585337 Gitelman Syndrome: A Rare Case of Hypokalaemia and a Novel Mutation. 2021 1
2 33890260 [Sectio Caesarea under Gitelman Syndrome]. 2021 Apr 1
3 32292023 Gitelman syndrome associated with chondrocalcinosis and severe neuropathy: a novel heterozygous mutation in SLC12A3 gene. 2020 Apr 10 1
4 26770037 Mutations in SLC12A3 and CLCNKB and Their Correlation with Clinical Phenotype in Patients with Gitelman and Gitelman-like Syndrome. 2016 Jan 1
5 28124936 [Gitelman´s syndrome as common cause of hypokalemia and hypomagnesemia]. 2016 Winter 1
6 24645554 [Potassium-preserving properties of magnesium]. 2013 1