CLCN2 chloride channel mutations in familial hyperaldosteronism type II
Ute I. Scholl(Berlin Institute of Health at Charité - Universitätsmedizin Berlin), Gabriel Stölting(Forschungszentrum Jülich), Julia Schewe(Heinrich Heine University Düsseldorf), Anne Thiel(Heinrich Heine University Düsseldorf), Hua Tan(Forschungszentrum Jülich), Carol Nelson‐Williams(Howard Hughes Medical Institute), Alfred A. Vichot(Howard Hughes Medical Institute), Sheng Chih Jin(Yale University), Erin Loring(Howard Hughes Medical Institute), Verena Untiet(Forschungszentrum Jülich), Taekyeong Yoo(Seoul National University), Jungmin Choi(Howard Hughes Medical Institute), Shengxin Xu(The University of Queensland), Aihua Wu(The University of Queensland), Marieluise Kirchner(Max Delbrück Center), Philipp Mertins(Max Delbrück Center), Lars Christian Rump(Heinrich Heine University Düsseldorf), Ali Mirza Onder(Le Bonheur Children's Hospital), Cory Gamble(Cooper Clinic), Daniel W. McKenney(Peyton Manning Children’s Hospital at St.Vincent), Robert W. Lash(University of Michigan), Deborah P. Jones(Vanderbilt University), G. Chune(Olin E. Teague Veterans Medical Center), Priscila Gagliardi(Nemours Children’s Clinic), Murim Choi(Seoul National University), Richard D. Gordon(The University of Queensland), Michael Stowasser(The University of Queensland), Christoph Fahlke(Forschungszentrum Jülich), Richard P. Lifton(Howard Hughes Medical Institute)
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