Discordant Genotype-Phenotype Correlation in Familial Hyperaldosteronism Type III with KCNJ5 Gene Mutation: A Patient Report and Review of the Literature-Reference-Cited by-同舟云学术

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Discordant Genotype-Phenotype Correlation in Familial Hyperaldosteronism Type III with KCNJ5 Gene Mutation: A Patient Report and Review of the Literature

Published:2014 Issue:2 Volume:82 Page:138-142
ISSN:1663-2818
Container-title:Hormone Research in Paediatrics
language:en
Short-container-title:Horm Res Paediatr

Author:

Adachi Masanori,Muroya Koji,Asakura Yumi,Sugiyama Kenji,Homma Keiko,Hasegawa Tomonobu

Publisher

S. Karger AG

Subject

Endocrinology,Endocrinology, Diabetes and Metabolism,Pediatrics, Perinatology, and Child Health

Cited by 34 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. Familial hyperaldosteronism: an European Reference Network on Rare Endocrine Conditions clinical practice guideline;European Journal of Endocrinology;2024-03-30

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

3. Primary Aldosteronism;Endocrinology;2023

4. Primary Aldosteronism;Endocrinology;2023

5. Disorders of the adrenal cortex: Genetic and molecular aspects;Frontiers in Endocrinology;2022-08-29

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