Mutations in the chloride channel gene, CLCNKB, cause Bartter's syndrome type III
David B. Simon(Howard Hughes Medical Institute), Richard P. Lifton(Rockefeller University), Érica Mendonça(Hospital de Santa Maria), Carol M. Taylor(Birmingham Children's Hospital), Howard Trachtman(University of Michigan), Carol Nelson‐Williams(Howard Hughes Medical Institute), José Manuel Morales(Hospital Universitario 12 De Octubre), Ranjit S. Bindra(Yale University), Harika Alpay(Marmara University), William R. Griswold(Boston Children's Hospital), Scott J. Schurman(Johns Hopkins University), Rosário Stone(Hospital de Santa Maria), Ahmet Nayır(Istanbul University), Traci A. Mansfield(Howard Hughes Medical Institute), George A. Richard(University of Florida), Andrew S. Brem(Providence College), Eunice John(University of Illinois Chicago), Daniela T. Pilz(University Hospital of Wales), A Bakkaloğlu(Hacettepe University Hospital), Juan Rodríguez‐Soriano(Hospital de Cruces), Sami A. Sanjad(King Faisal Specialist Hospital & Research Centre)
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