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
|