Skip to main navigation Skip to search Skip to main content

CLCN2 chloride channel mutations in familial hyperaldosteronism type II

  • Ute I. Scholl*
  • , Gabriel Stölting
  • , Julia Schewe
  • , 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
*Corresponding author for this work

Research output: Contribution to journalArticlepeer-review

Fingerprint

Dive into the research topics of 'CLCN2 chloride channel mutations in familial hyperaldosteronism type II'. Together they form a unique fingerprint.
Sort by

Keyphrases

Biochemistry, Genetics and Molecular Biology