Genetic heterogeneity of Barter's syndrome revealed by mutations in the K+ channel, ROMK
David B. Simon(Howard Hughes Medical Institute), Richard P. Lifton(Rockefeller University), Fiona E. Karet(Howard Hughes Medical Institute), Jahed Hamdan(Dhahran Health Center), Antonio DiPietro(Ospedale Antonio Cardarelli), Sami A. Sanjad(King Faisal Specialist Hospital & Research Centre), Juan Rodríguez‐Soriano(Hospital de Cruces), Howard Trachtman(University of Michigan)
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