Publication year
1999Author(s)
Number of pages
9 p.
Source
American Journal of Human Genetics, 64, 1, (1999), pp. 180-188ISSN
Publication type
Article / Letter to editor
Display more detailsDisplay less details
Organization
Paediatrics - OUD tm 2017
Human Genetics
Journal title
American Journal of Human Genetics
Volume
vol. 64
Issue
iss. 1
Page start
p. 180
Page end
p. 188
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 syndroomThis item appears in the following Collection(s)
- Academic publications [246642]
- Faculty of Medical Sciences [93380]
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