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Title: Hereditary isolated renal magnesium loss maps to chromosome 11q23
Author(s): Meij, I.C.; Saar, K.; Heuvel, L.P.W.J. van den ; Nuernberg, G.; Volmer, M.; Hildebrandt, F.; Reis, A.; Monnens, L.A.H. ; Knoers, N.V.A.M.
Publication year: 1999
Source: American Journal of Human Genetics, vol. 64, iss. 1, (1999), pp. 180-188
Number of Pages: 9 p.
ISSN: 0002-9297
DOI: https://doi.org/10.1086/302199
Publication type: Article / Letter to editor

Please use this identifier to cite or link to this item : https://hdl.handle.net/2066/184786   https://hdl.handle.net/2066/184786

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Subject: Heriditary disorders of magnesiumtransport. Genetic localisation and pathophysiology.
Identification of the gene defects in Bartter syndrome and Gitelman syndrome
Aangeboren stoornissen in magnesiumtransport. Genetica en Pathophysiologie.
Identificatie van de gen defecten in Bartter syndroom en Gitelman syndroom
Organization: Paediatrics
Human Genetics
Journal title:
American Journal of Human Genetics
Volume: vol. 64
Issue: iss. 1
Page start: p. 180
Page end: p. 188

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