Mutations in the gene encoding the inwardly-rectifying renal potassium channel, ROMK, cause the antenatal variant of Bartter syndrome: evidence for genetic heterogeneity. International Collaborative Study Group for Bartter-like Syndromes [published erratum appears in Hum Mol Genet 1997 Apr;6(4):650]

Lothar Károlyi; Steven Hébert; Christian Wieg; Pascal Saunier; Patrick Niaudet; Lisa M. Guay‐Woodford; Georges Deschênes; L.A.H. Monnens; Jean‐Luc Alessandri; Andreas Ziegler; Gilbert Madrigal; M Deschaux; Willem Proesmans; Emmanuel Cougoureux; Lionel Forestier; Corinne Antignac; Arnold Köckerling; D Zimmermann; Martin Vollmer; Henny H. Lemmink; Christopher J. Wright; Frederique Lorridon; Louis David; Delphine Feldmann; Bernd Roth; Manuela C. Koch; Rosa Vargas; Karl‐Heinz Grzeschik; Willy M. Nillesen; Friedhelm Hildebrandt; Nine Knoers; Martin Konrad; Hannsjörg W. Seyberth; Gian Franco Rizzoni; Lambertus P. van den Heuvel; G Jean; M. Brandis

doi:10.1093/hmg/6.1.17

Mutations in the gene encoding the inwardly-rectifying renal potassium channel, ROMK, cause the antenatal variant of Bartter syndrome: evidence for genetic heterogeneity. International Collaborative Study Group for Bartter-like Syndromes [published erratum appears in Hum Mol Genet 1997 Apr;6(4):650]

Lothar Károlyi(Philipps University of Marburg), Steven Hébert(Brigham and Women's Hospital), Christian Wieg(Boston Children's Hospital), Pascal Saunier(Sorbonne Université), Patrick Niaudet(Hôpital Necker-Enfants Malades), Lisa M. Guay‐Woodford(Children's Hospital of Philadelphia), Georges Deschênes(Hôpital Robert-Debré), L.A.H. Monnens(Radboud University Nijmegen), Jean‐Luc Alessandri(University of Reunion Island), Andreas Ziegler(Universität Hamburg), Gilbert Madrigal(Brigham and Women's Hospital), M Deschaux(Inserm), Willem Proesmans(KU Leuven), Emmanuel Cougoureux(Sorbonne Université), Lionel Forestier(Inserm), Corinne Antignac(Hôpital Necker-Enfants Malades), Arnold Köckerling(Philipps University of Marburg), D Zimmermann(Philipps University of Marburg), Martin Vollmer(University Medical Center Freiburg), Henny H. Lemmink(University Medical Center Groningen), Christopher J. Wright(Oxford Nanopore Technologies (United Kingdom)), Frederique Lorridon(Sorbonne Université), Louis David(Clinique Les Fontaines), Delphine Feldmann(Hôpital Armand-Trousseau), Bernd Roth(German Society of Medical Intensive Care and Emergency Medicine), Manuela C. Koch(Philipps University of Marburg), Rosa Vargas(Inserm), Karl‐Heinz Grzeschik, Willy M. Nillesen(Radboud University Nijmegen), Friedhelm Hildebrandt(NIHR Newcastle Biomedical Research Centre), Nine Knoers(University Medical Center Utrecht), Martin Konrad(University Hospital Münster), Hannsjörg W. Seyberth(Philipps University of Marburg), Gian Franco Rizzoni(Boston Children's Hospital), Lambertus P. van den Heuvel(Radboud University Nijmegen), G Jean(Inserm), M. Brandis(Indiana University School of Medicine)

Human Molecular Genetics

January 1, 1997

10.1093/hmg/6.1.17

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