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2. Mutations in the gene encoding the inwardly-rectifying renal potassium channel, ROMK, cause the antenatal variant of Barrter syndrome : evidence for genetic heterogeneity

Author

Károlyi, L., Konrad, M., Köckerling, A., Ziegler, A., Zimmermann, D.K., Roth, B., Wieg, C., Grzeschik, K.H., Koch, M.C., Seyberth, H.W., Vargas, R., Forestier, C., Jean, G., Deschaux, M., Rizzoni, G.F., Niaudet, P., Antignac, C., Feldmann, D., Lorridon, F., Cougoureux, E., Laroze, F., Alessandri, J.-L., David, L., Saunier, P., Deschenes, G., Hildebrandt, F., Vollmer, M., Proesmans, W., Brandis, M., Heuvel, L.P.W.J. van den, Lemmink, H.H., Nillesen, W., Monnens, L.A.H., Knoers, N.V.A.M., Guay-Woodford, L.M., Wright, C.J., Madrigal, G., and Hebert, S.C.

Subjects
Cultured, Ion Transport, Cells, Molecular, Molecular Probe Techniques, Hospitalized, Kidney, Kidney Function Tests, Urogenital Abnormalities (Non MeSH), Basement Membrane, Urethra, Urethral Diseases, Cell Adhesion, Kidney Diseases, Endothelium, Cloning, Molecular, Child, Gram-Negative Bacterial Infections, GeneralLiterature_REFERENCE(e.g.,dictionaries,encyclopedias,glossaries), Child, Hospitalized, Peritoneal Dialysis, Cells, Cultured, Cloning
Abstract

Contains fulltext : 24466___.PDF (Publisher’s version ) (Open Access)

Published
1997

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