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.