Skip to search formSkip to main contentSkip to account menu

Familial Hyperaldosteronism Type 3

Familial hyperaldosteronism caused by a mutation in the KCNJ5 gene, which encodes the inwardly rectifying potassium channel. This condition… 
National Institutes of Health

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
Review
2014
Review
2014
Channels and pumps in aldosterone-producing adenomas.
Primary aldosteronism is the most common cause of secondary hypertension, with a prevalence of about 5% of the general… 
By clicking accept or continuing to use the site, you agree to the terms outlined in our Privacy Policy (opens in a new tab), Terms of Service (opens in a new tab), and Dataset License (opens in a new tab)