Active intestinal chloride secretion in human carriers of cystic fibrosis mutations: An evaluation of the hypothesis that heterozygotes have subnormal active intestinal chloride secretion

C. Hogenauer, C. A. Santa Ana, J. L. Porter, M. Millard, A. Gelfand, R. L. Rosenblatt, C. B. Prestidge, J. S. Fordtran

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Medicine & Life Sciences