A Novel Y152C KCNJ5 Mutation Responsible for Familial Hyperaldosteronism Type III-Reference-Cited by-同舟云学术

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A Novel Y152C KCNJ5 Mutation Responsible for Familial Hyperaldosteronism Type III

Published:2013-11 Issue:11 Volume:98 Page:E1861-E1865
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,Hattangady Namita G.,Penton David,Isales Carlos M.,Edwards Michael A.,Williams Tracy A.,Sterner Christina,Warth Richard,Mulatero Paolo,Rainey William E.

Publisher

The Endocrine Society

Subject

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

Cited by 88 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. Diagnosis and management of resistant hypertension;BMJ;2024-06-19

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

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

4. Differences in the clinical and hormonal presentation of patients with familial and sporadic primary aldosteronism;Frontiers in Endocrinology;2024-03-01

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

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