A case of pseudohypoaldosteronism type 1 with a mutation in the mineralocorticoid receptor gene-Reference-Cited by-同舟云学术

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A case of pseudohypoaldosteronism type 1 with a mutation in the mineralocorticoid receptor gene

Published:2011 Issue:2 Volume:54 Page:90
ISSN:1738-1061
Container-title:Korean Journal of Pediatrics
language:en
Short-container-title:Korean J Pediatr

Author:

Lee Se Eun¹,Jung Yun Hye¹,Han Kyoung Hee¹,Lee Hyun Kyung¹,Kang Hee Gyung¹²,Ha Il Soo¹³,Choi Yong⁴,Cheong Hae Il¹²³

Affiliation:

1. Department of Pediatrics, Seoul National University Children's Hospital, Seoul, Korea.

2. Research Center for Rare Diseases, Seoul National University Hospital, Seoul, Korea.

3. Kidney Research Institute, Medical Research Center, Seoul National University College of Medicine, Seoul, Korea.

4. Department of Pediatrics, Inje University Haeundae Paik Hospital, Busan, Korea.

Publisher

Korean Pediatric Society

Subject

Pediatrics,Pediatrics, Perinatology, and Child Health

Link

http://kjp.or.kr/upload/pdf/kjped-54-90.pdf

Reference23 articles.

1. Inactivating mutations of the mineralocorticoid receptor in Type I pseudohypoaldosteronism

2. Mineralocorticoid resistance

3. Type I Pseudohypoaldosteronism Includes Two Clinically and Genetically Distinct Entities with either Renal or Multiple Target Organ Defects

4. Mutations in the mineralocorticoid receptor gene cause autosomal dominant pseudohypoaldosteronism type I

Cited by 9 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. Pseudohypoaldosteronism Type 1 with a Novel Mutation in the NR3C2 Gene: A Case Report;Childhood Kidney Diseases;2020-04-30

2. Transient Pseudohypoaldosteronism in an Infant: A Case Report;Journal of the ASEAN Federation of Endocrine Societies;2018-04-12

3. Mineralocorticoid Deficiency;Endocrinology: Adult and Pediatric;2016

4. Pseudohypoaldosteronism in a newborn male with functional polymorphisms in the mineralocorticoid receptor genes;Annals of Pediatric Endocrinology & Metabolism;2015

5. Pseudohypoaldosteronism Type 1;Journal of Genetic Medicine;2013-12-31

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