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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
- Department of Genetics
- Roy and Diana Vagelos Division of Biology & Biomedical Sciences (DBBS)
- Institute of Clinical and Translational Sciences (ICTS)
- NeuroGenomics and Informatics Center
- Center of Regenerative Medicine
- DBBS - Computational and Systems Biology
- DBBS - Neurosciences
- DBBS - Human and Statistical Genetics
- DBBS - Molecular Genetics and Genomics
- Hope Center for Neurological Disorders
- Intellectual and Developmental Disabilities Research Center (IDDRC)
Research output: Contribution to journal › Article › peer-review
197
Scopus
citations