Liddle syndrome: clinical and genetic profiles-Reference-Cited by-同舟云学术

Liddle syndrome: clinical and genetic profiles

Published:2016-11-29 Issue:5 Volume:19 Page:524-529
ISSN:1524-6175
Container-title:The Journal of Clinical Hypertension
language:en
Short-container-title:J Clin Hypertens

Author:

Cui Yunying¹,Tong Anli¹,Jiang Jun²,Wang Fen¹,Li Chunyan¹

Affiliation:

1. Department of Endocrinology; Key Laboratory of Endocrinology; Ministry of Health; Peking Union Medical College Hospital (PUMCH); Chinese Academy of Medical Sciences; Beijing China

2. The Key Laboratory of Genome Sciences and Information; Beijing Institute of Genomics; Chinese Academy of Sciences; Beijing China

Funder

National Key Program of Clinical Science of China

Publisher

Wiley

Subject

Cardiology and Cardiovascular Medicine,Endocrinology, Diabetes and Metabolism,Internal Medicine

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1111/jch.12949/fullpdf

Reference12 articles.

1. The ENaC channel as the primary determinant of two human diseases: Liddle syndrome and pseudohypoaldosteronism;Schild;Nephrologie,1996

2. A familial renal disorder simulating primary aldosteronism but with negligible aldosterone secretion;Liddle;Trans Assoc Am Physicians,1963

3. Prevalence of Liddle syndrome among young hypertension patients of undetermined cause in a Chinese population;Wang;J Clin Hypertens,2015

4. Phenotype-genotype analysis in two Chinese families with Liddle syndrome;Gong;Mol Biol Rep,2014

5. Mutations and variants of the epithelial sodium channel gene in Liddle's syndrome and primary hypertension;Melander;Hypertension,1998

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