Literature DB >> 29479080

Hypertension: CLCN2 chloride channel mutations in primary aldosteronism.

Susan J Allison.   

Abstract

Entities:  

Mesh：

Substances：

Year:  2018        PMID： 29479080     DOI： 10.1038/nrneph.2018.17

Source DB:  PubMed          Journal:  Nat Rev Nephrol        ISSN： 1759-5061            Impact factor:   28.314


× No keyword cloud information.
  2 in total

1.  A gain-of-function mutation in the CLCN2 chloride channel gene causes primary aldosteronism.

Authors:  Fabio L Fernandes-Rosa; Georgios Daniil; Ian J Orozco; Corinna Göppner; Rami El Zein; Vandana Jain; Sheerazed Boulkroun; Xavier Jeunemaitre; Laurence Amar; Hervé Lefebvre; Thomas Schwarzmayr; Tim M Strom; Thomas J Jentsch; Maria-Christina Zennaro
Journal:  Nat Genet       Date:  2018-02-05       Impact factor: 38.330

2.  CLCN2 chloride channel mutations in familial hyperaldosteronism type II.

Authors:  Gabriel Stölting; Julia Schewe; Ute I Scholl; Anne Thiel; Hua Tan; Carol Nelson-Williams; Alfred A Vichot; Sheng Chih Jin; Erin Loring; Verena Untiet; Taekyeong Yoo; Jungmin Choi; Shengxin Xu; Aihua Wu; Marieluise Kirchner; Philipp Mertins; Lars C Rump; Ali Mirza Onder; Cory Gamble; Daniel McKenney; Robert W Lash; Deborah P Jones; Gary Chune; Priscila Gagliardi; Murim Choi; Richard Gordon; Michael Stowasser; Christoph Fahlke; Richard P Lifton
Journal:  Nat Genet       Date:  2018-02-05       Impact factor: 38.330
  2 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.