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  4. Response to letter to the editor: “Adrenalectomy completely cured hypertension in familial hyperaldosteronism type I patients with somatic KCNJ5 mutation”
 
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Response to letter to the editor: “Adrenalectomy completely cured hypertension in familial hyperaldosteronism type I patients with somatic KCNJ5 mutation”

Journal
Journal of Clinical Endocrinology and Metabolism
Journal Volume
105
Journal Issue
5
Pages
dgz110
Date Issued
2020
Author(s)
Lin, Yu-Fang
Peng, Kang-Yung
Chang, Chia-Hui
Hu, Ya-Hui
VIN-CENT WU  
SHIH-CHIEH CHUEH  
DOI
10.1210/clinem/dgz110
URI
https://www.scopus.com/inward/record.uri?eid=2-s2.0-85082542566&doi=10.1210%2fclinem%2fdgz110&partnerID=40&md5=f0c141dba9b578055ccbc8f37e651ea9
https://scholars.lib.ntu.edu.tw/handle/123456789/514970
SDGs

[SDGs]SDG3

Other Subjects
aldosterone; renin; G protein coupled inwardly rectifying potassium channel; KCNJ5 protein, human; adrenalectomy; aldosterone blood level; biochemical analysis; biochemical composition; clinical feature; familial disease; human; hyperaldosteronism; hypertension; KCNJ5 gene; Letter; outcome assessment; phenotypic variation; plasma renin activity; postoperative period; prediction; priority journal; somatic mutation; treatment response; adrenalectomy; genetics; mutation; adrenal tumor; familial hyperaldosteronism type I; gene; mutational analysis; phenotype; primary hyperaldosteronism; surgical patient; treatment outcome; treatment response; Adrenalectomy; G Protein-Coupled Inwardly-Rectifying Potassium Channels; Humans; Hyperaldosteronism; Hypertension; Mutation
Publisher
Endocrine Society
Type
letter

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