A Case of Severe Hyperaldosteronism Caused by a De Novo Mutation Affecting a Critical Salt Bridge Kir3.4 Residue-Reference-Cited by-同舟云学术

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A Case of Severe Hyperaldosteronism Caused by a De Novo Mutation Affecting a Critical Salt Bridge Kir3.4 Residue

Published:2015-01 Issue:1 Volume:100 Page:E114-E118
ISSN:0021-972X
Container-title:The Journal of Clinical Endocrinology & Metabolism
language:en
Short-container-title:The Journal of Clinical Endocrinology & Metabolism

Author:

Monticone Silvia,Bandulik Sascha,Stindl Julia,Zilbermint Mihail,Dedov Ivan,Mulatero Paolo,Allgaeuer Michael,Lee Chyi-Chia Richard,Stratakis Constantine A.,Williams Tracy A.,Tiulpakov Anatoly

Publisher

The Endocrine Society

Subject

Biochemistry, medical,Clinical Biochemistry,Endocrinology,Biochemistry,Endocrinology, Diabetes and Metabolism

Cited by 52 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. KCNJ5 mutations in familial and non-familial primary aldosteronism;European Journal of Endocrinology;2024-05-23

2. GEMIN4 Variants: Risk Profiling, Bioinformatics, and Dynamic Simulations Uncover Susceptibility to Bladder Carcinoma;Archives of Medical Research;2024-04

3. Familial hyperaldosteronism: an European Reference Network on Rare Endocrine Conditions clinical practice guideline;European Journal of Endocrinology;2024-03-30

4. Primary aldosteronism: molecular medicine meets public health;Nature Reviews Nephrology;2023-08-23

5. O tempora, o mores;JACC: Asia;2023-08

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