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