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. CougoureuxF. 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 Statistic

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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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",

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 - http://www.scopus.com/inward/record.url?scp=0030893550&partnerID=8YFLogxK

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))

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