
pmid: 11068641
handle: 2066/258640
Item does not contain fulltext
Hypocalcemia, Identificatie van de gen defecten in Bartter syndroom en Gitelman syndroom, Genetic Diseases, Inborn, Biological Transport, Identification of the gene defects in Bartter syndrome and Gitelman syndrome, Aangeboren stoornissen in magnesiumtransport. Genetica en Pathophysiologie., Nephrocalcinosis, Humans, Calcium, Magnesium, Heriditary disorders of magnesiumtransport. Genetic localisation and pathophysiology., Metabolism, Inborn Errors
Hypocalcemia, Identificatie van de gen defecten in Bartter syndroom en Gitelman syndroom, Genetic Diseases, Inborn, Biological Transport, Identification of the gene defects in Bartter syndrome and Gitelman syndrome, Aangeboren stoornissen in magnesiumtransport. Genetica en Pathophysiologie., Nephrocalcinosis, Humans, Calcium, Magnesium, Heriditary disorders of magnesiumtransport. Genetic localisation and pathophysiology., Metabolism, Inborn Errors
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