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"HYPERALDOSTERONISM," "FAMILIAL," TYPE III
- ... TYPE I; HALD1 HYPERALDOSTERONISM, FAMILIAL, TYPE II; HALD2 HYPERALDOSTERONISM, FAMILIAL, TYPE III; HALD3 PubMed Funder JW. The genetic basis of ... WE. a Novel Y152C KCNJ5 mutation responsible for familial hyperaldosteronism type III. J Clin Endocrinol Metab. 2013 Nov;98(11): ...
- ... gene mutations have been identified in people with familial hyperaldosteronism type III. These mutations, known as germline mutations, are found ... WE. a Novel Y152C KCNJ5 mutation responsible for familial hyperaldosteronism type III. J Clin Endocrinol Metab. 2013 Nov;98(11): ...
- ... gene detected in patients with aldosterone synthase deficiency type I: ... Rump LC. Familial hyperaldosteronism I-III. Horm Metab Res. 2010 Jun;42(6):424- ...
- ... A genetic change affecting the CYP11B1 gene causes familial hyperaldosteronism type I, a disorder that leads to hypertension. This ... production, which leads to the hypertension associated with familial hyperaldosteronism type I. More About This Health Condition C11B1_HUMAN ...