Molecular cloning, tissue distribution, chromosomal mapping and linkage analysis in idiopathic hypercalciuria of the human epithelial calcium channel
Publication year
2000Author(s)
Number of pages
6 p.
Source
Genomics : International Journal of Gene Mapping and Nucleotide Sequencing Emphasizing Analyses of the Human and Other Complex Genomes, 67, (2000), pp. 48-53ISSN
Publication type
Article / Letter to editor

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Organization
Cell Physiology
Physiology
Paediatrics - OUD tm 2017
Human Genetics
Journal title
Genomics : International Journal of Gene Mapping and Nucleotide Sequencing Emphasizing Analyses of the Human and Other Complex Genomes
Volume
vol. 67
Page start
p. 48
Page end
p. 53
Subject
Heriditary disorders of magnesiumtransport. Genetic localisation and pathophysiology.; Identification of the gene defects in Bartter syndrome and Gitelman syndrome; Regulation of salt and water reabsorption in the renal collecting duct; Aangeboren stoornissen in magnesiumtransport. Genetica en Pathophysiologie.; Identificatie van de gen defecten in Bartter syndroom en Gitelman syndroom; Regulatie water en zouttransport in de verzamelbuis van de nierThis item appears in the following Collection(s)
- Academic publications [233366]
- Faculty of Medical Sciences [89127]
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