A novel <i>SCNN1A</i> variation in a patient with autosomal-recessive pseudohypoaldosteronism type 1-Reference-Cited by-同舟云学术

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A novel SCNN1A variation in a patient with autosomal-recessive pseudohypoaldosteronism type 1

Published:2021-04-08 Issue:0 Volume:0 Page:0-0
ISSN:1308-5727
Container-title:Journal of Clinical Research in Pediatric Endocrinology
language:
Short-container-title:Jcrpe

Author:

Huneif Mohammed Ayed,AlHazmy Ziyad Hamad,Shoomi Anas M.,AlGhofely Mohammed A.,Heena Humariya,Mushiba Aziza M.,AlSaheel Abdulhamid

Publisher

Galenos Yayinevi

Subject

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

Cited by 4 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. Pulmonary manifestations of Pseudohypoaldosteronism type 1b: A systematic review of the literature;Paediatric Respiratory Reviews;2024-09

2. Pseudohypoaldosteronism Type 1B and Cohen Syndrome: Novel Mutation, Unusual Combination, and Presentation;Cureus;2024-03-29

3. The Epithelial Sodium Channel—An Underestimated Drug Target;International Journal of Molecular Sciences;2023-04-24

4. Mineralocorticoid Receptor Activation in Vascular Insulin Resistance and Dysfunction;International Journal of Molecular Sciences;2022-08-11

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