Erratum: Mutations in the gene encoding the inwardly-rectifying renal potassium channel, ROMK, cause the antenatal variant of Bartter syndrome: Evidence for genetic heterogeneity (Human Molecular Genetics (1997) 6 (17-26))

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

Erratum: Mutations in the gene encoding the inwardly-rectifying renal potassium channel, ROMK, cause the antenatal variant of Bartter syndrome: Evidence for genetic heterogeneity (Human Molecular Genetics (1997) 6 (17-26))

L. Karolyi
, M. Konrad
, A. Kockerling
, A. Ziegler
, D. K. Zimmermann
, B. Roth
, C. Wieg
, K. H. Grzeschik
, M. C. Koch
, H. W. Seyberth
, R. Vargas
, L. Forestier
, G. Jean
, M. Deschaux
, G. F. Rizzoni
, P. Niaudet
, C. Antignac
, D. Feldmann
, F. Lorridon
, E. Cougoureux

F. Laroze, J. L. Alessandri, L. David, P. Saunier, G. Deschenes, F. Hildebrandt, M. Vollmer, W. Proesmans, M. Brandis, L. P.W.J. Van den Heuvel, H. H. Lemmink, W. Nillesen, L. A.H. Monnens, N. V.A.M. Knoers, L. M. Guay-Woodford, C. J. Wright, G. Madrigal, S. C. Hebert

Institute of Medical Biometry and Statistics

Original language	English
Journal	Human Molecular Genetics
Volume	6
Issue number	4
Pages (from-to)	650
Number of pages	1
ISSN	0964-6906
Publication status	Published - 1997

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This output contributes to the following UN Sustainable Development Goals (SDGs)

SDG 3 Good Health and Well-being

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Karolyi, L., Konrad, M., Kockerling, A., Ziegler, A., Zimmermann, D. K., Roth, B., Wieg, C., Grzeschik, K. H., Koch, M. C., Seyberth, H. W., Vargas, R., Forestier, L., Jean, G., Deschaux, M., Rizzoni, G. F., Niaudet, P., Antignac, C., Feldmann, D., Lorridon, F., ... Hebert, S. C. (1997). Erratum: Mutations in the gene encoding the inwardly-rectifying renal potassium channel, ROMK, cause the antenatal variant of Bartter syndrome: Evidence for genetic heterogeneity (Human Molecular Genetics (1997) 6 (17-26)). Human Molecular Genetics, 6(4), 650.

@article{2db81152115345f8a55abf38322417f8,

title = "Erratum: Mutations in the gene encoding the inwardly-rectifying renal potassium channel, ROMK, cause the antenatal variant of Bartter syndrome: Evidence for genetic heterogeneity (Human Molecular Genetics (1997) 6 (17-26))",

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

year = "1997",

language = "English",

volume = "6",

pages = "650",

journal = "Human Molecular Genetics",

issn = "0964-6906",

publisher = "Oxford University Press",

number = "4",

}

Karolyi, L, Konrad, M, Kockerling, A, Ziegler, A, Zimmermann, DK, Roth, B, Wieg, C, Grzeschik, KH, Koch, MC, Seyberth, HW, Vargas, R, Forestier, L, Jean, G, Deschaux, M, Rizzoni, GF, Niaudet, P, Antignac, C, Feldmann, D, Lorridon, F, Cougoureux, E, Laroze, F, Alessandri, JL, David, L, Saunier, P, Deschenes, G, Hildebrandt, F, Vollmer, M, Proesmans, W, Brandis, M, Van den Heuvel, LPWJ, Lemmink, HH, Nillesen, W, Monnens, LAH, Knoers, NVAM, Guay-Woodford, LM, Wright, CJ, Madrigal, G & Hebert, SC 1997, 'Erratum: Mutations in the gene encoding the inwardly-rectifying renal potassium channel, ROMK, cause the antenatal variant of Bartter syndrome: Evidence for genetic heterogeneity (Human Molecular Genetics (1997) 6 (17-26))', Human Molecular Genetics, vol. 6, no. 4, pp. 650.

Erratum: Mutations in the gene encoding the inwardly-rectifying renal potassium channel, ROMK, cause the antenatal variant of Bartter syndrome: Evidence for genetic heterogeneity (Human Molecular Genetics (1997) 6 (17-26)). / Karolyi, L.; Konrad, M.; Kockerling, A. et al.
In: Human Molecular Genetics, Vol. 6, No. 4, 1997, p. 650.

Research output: Journal Articles › Comments/Debates

TY - JOUR

T1 - Erratum: Mutations in the gene encoding the inwardly-rectifying renal potassium channel, ROMK, cause the antenatal variant of Bartter syndrome: Evidence for genetic heterogeneity (Human Molecular Genetics (1997) 6 (17-26))

AU - Karolyi, L.

AU - Konrad, M.

AU - Kockerling, A.

AU - Ziegler, A.

AU - Zimmermann, D. K.

AU - Roth, B.

AU - Wieg, C.

AU - Grzeschik, K. H.

AU - Koch, M. C.

AU - Seyberth, H. W.

AU - Vargas, R.

AU - Forestier, L.

AU - Jean, G.

AU - Deschaux, M.

AU - Rizzoni, G. F.

AU - Niaudet, P.

AU - Antignac, C.

AU - Feldmann, D.

AU - Lorridon, F.

AU - Cougoureux, E.

AU - Laroze, F.

AU - Alessandri, J. L.

AU - David, L.

AU - Saunier, P.

AU - Deschenes, G.

AU - Hildebrandt, F.

AU - Vollmer, M.

AU - Proesmans, W.

AU - Brandis, M.

AU - Van den Heuvel, L. P.W.J.

AU - Lemmink, H. H.

AU - Nillesen, W.

AU - Monnens, L. A.H.

AU - Knoers, N. V.A.M.

AU - Guay-Woodford, L. M.

AU - Wright, C. J.

AU - Madrigal, G.

AU - Hebert, S. C.

PY - 1997

Y1 - 1997

UR - https://www.scopus.com/pages/publications/0030893550

M3 - Comments/Debates

AN - SCOPUS:0030893550

SN - 0964-6906

VL - 6

SP - 650

JO - Human Molecular Genetics

JF - Human Molecular Genetics

IS - 4

ER -

Erratum: Mutations in the gene encoding the inwardly-rectifying renal potassium channel, ROMK, cause the antenatal variant of Bartter syndrome: Evidence for genetic heterogeneity (Human Molecular Genetics (1997) 6 (17-26))

UN SDGs

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