Literature DB >> 27026694

A novel mutation in KLHL3 gene causes familial hyperkalemic hypertension.

D Kelly1, M R Rodzlan2, X Jeunemaitre3, C Wall2.   

Abstract

Entities:  

Year:  2016        PMID： 27026694     DOI： 10.1093/qjmed/hcw043

Source DB:  PubMed          Journal:  QJM        ISSN： 1460-2393


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  1 in total

1.  A case report of pseudohypoaldosteronism type II with a homozygous KLHL3 variant accompanied by hyperthyroidism.

Authors:  Rui Zhang; Simin Zhang; Yingying Luo; Meng Li; Xin Wen; Xiaoling Cai; Xueyao Han; Linong Ji
Journal:  BMC Endocr Disord       Date:  2021-05-22       Impact factor: 2.763
  1 in total

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