Mutations in the gene encoding the inwardly-rectifying renal potassium channel, ROMK, cause the antenatal variant of Bartter syndrome: Evidence for genetic heterogeneity

Lothar Károlyi, Martin Konrad, Arnold Köckerling, Andreas Ziegler, Dorthe K. Zimmermann, Bernd Roth, Christian Wieg, Karl Heinz Grzeschik, Manuela C. Koch, Hannsjörg W. Seyberth, Rosa Vargas, Lionel Forestier, Genevieve Jean, Michele Deschaux, Gian Franco Rizzoni, Patrick Niaudet, Corinne Antignac, Delphine Feldmann, Frederique Lorridon, Emmanuel CougoureuxFrance Laroze, Jean Luc Alessandri, Louis David, Pascal Saunier, Georges Deschenes, Friedhelm Hildebrandt, Martin Vollmer, Willem Proesmans, Matthias Brandis, Lambertus P.W.J. Van Den Heuvel, Henny H. Lemmink, Willy Nillesen, Leo A.H. Monnens, Nine V.A.M. Knoers, Lisa M. Guay-Woodford*, Christopher J. Wright, Gilbert Madrigal, Steven C. Hebert

*Corresponding author for this work
176 Citations (Scopus)

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