Normal fibrinolytic responses to 1-desamino-8-D-arginine vasopressin in patients with nephrogenic diabetes insipidus caused by mutations in the aquaporin-2 gene
Publication year
1996Source
Nephron, 72, (1996), pp. 544-546ISSN
Publication type
Article / Letter to editor

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Organization
Paediatrics - OUD tm 2017
Human Genetics
Journal title
Nephron
Volume
vol. 72
Page start
p. 544
Page end
p. 546
Subject
Elucidation of the molecular defect responsible for congenital nephrogenic diabetes insipidus (NDI); Opheldering van het moleculaire defect dat verantwoordelijk is voor congenitale nefrogene diabetes insipidus (NDI)This item appears in the following Collection(s)
- Academic publications [227248]
- Faculty of Medical Sciences [86732]
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