Disease: Hypomagnesemia ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0151723
Disease: Hypomagnesemia
Hypomagnesemia 		0.010 GeneticVariation phenotype BEFREE In this issue of the JCI, Glaudemans andcolleagues show that mutations in voltage-gated K+ channel subtype 1.1(Kv1.1) cause autosomal dominant hypomagnesemia in humans (see the related article beginning on page 936). 19348045 2009