Condition: Hyperaldosteronism, Familial, Type II


rs1085307938 in CLCN2 gene and Hyperaldosteronism, Familial, Type II PMID 29403012 2018 A gain-of-function mutation in the CLCN2 chloride channel gene causes primary aldosteronism.

PMID 29403011 2018 CLCN2 chloride channel mutations in familial hyperaldosteronism type II.

rs1553853557 in CLCN2;FAM131A gene and Hyperaldosteronism, Familial, Type II PMID 29403011 2018 CLCN2 chloride channel mutations in familial hyperaldosteronism type II.

PMID 29403012 2018 A gain-of-function mutation in the CLCN2 chloride channel gene causes primary aldosteronism.