Misfolded vasopressin V2 receptors caused by extracellular point mutations entail congenital nephrogenic diabetes insipidus.
Publication year
2000Source
Molecular and Cellular Endocrinology, 164, (2000), pp. 31-39ISSN
Publication type
Article / Letter to editor

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Organization
Human Genetics
Journal title
Molecular and Cellular Endocrinology
Volume
vol. 164
Page start
p. 31
Page end
p. 39
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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