Autosomal recessive nephrogenic diabetes insipidus caused by an aquaporin-2 mutation
Publication year
1997Author(s)
Number of pages
4 p.
Source
Journal of Clinical Endocrinology and Metabolism, 82, (1997), pp. 686-689ISSN
Publication type
Article / Letter to editor
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Organization
Paediatrics - OUD tm 2017
Human Genetics
Journal title
Journal of Clinical Endocrinology and Metabolism
Volume
vol. 82
Page start
p. 686
Page end
p. 689
Subject
Nephrogenic diabetes insipidus. Characterisation of the genmutation in vitro and in vivo - mechanism of action of DDAVP; Elucidation of the molecular defect responsible for congenital nephrogenic diabetes insipidus (NDI); Nephrogene diabetes insipidus: verdere karakterisering van de genmutatie met in vitro en in vivo expressie - de werking van DDAVP; Opheldering van het moleculaire defect dat verantwoordelijk is voor congenitale nefrogene diabetes insipidus (NDI)This item appears in the following Collection(s)
- Academic publications [243908]
- Faculty of Medical Sciences [92803]
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