Mutations in the chloride channel gene, CLCNKB, cause Bartter's syndrome type III

David B. Simon, Ranjit S. Bindra(Yale University), Traci A. Mansfield(Howard Hughes Medical Institute), Carol Nelson‐Williams(Howard Hughes Medical Institute), Érica Mendonça(Hospital de Santa Maria), Rosário Stone(Hospital de Santa Maria), Scott J. Schurman(Johns Hopkins All Children's Hospital), Ahmet Nayır(Istanbul University), Harika Alpay(Istanbul University), A Bakkaloğlu(Hacettepe University Hospital), Juan Rodríguez‐Soriano(Hospital de Cruces), José Manuel Morales(Hospital Universitario 12 De Octubre), Sami A. Sanjad(King Faisal Specialist Hospital & Research Centre), Carol M. Taylor(Birmingham Children's Hospital), Daniela T. Pilz(University Hospital of Wales), Andrew S. Brem(Providence College), Howard Trachtman(Albert Einstein College of Medicine), William R. Griswold(Boston Children's Hospital), George A. Richard(University of Florida), Eunice John(University of Illinois Chicago), Richard P. Lifton(Yale University)
Nature Genetics
October 1, 1997
Cited by 868

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