Condition: HYPERALDOSTERONISM, FAMILIAL, TYPE IV


rs759924732 in CACNA1H gene and HYPERALDOSTERONISM, FAMILIAL, TYPE IV PMID 27729216 2016 CACNA1H Mutations Are Associated With Different Forms of Primary Aldosteronism.

PMID 25907736 2015 Recurrent gain of function mutation in calcium channel CACNA1H causes early-onset hypertension with primary aldosteronism.