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Article

[Vasopressin type 2 receptor mutations in congenital diabetes insipidus].

Nihon rinsho. Japanese journal of clinical medicine - 1 Jul 1998

Tsukaguchi H, Matsubara H, Inada M

Abstract excerpt

Congenital nephrogenic diabetes insipidus is a rare inherited disorder, which is characterized by the inability of the kidney to concentrate urine due to unresponsiveness to antiduretic hormone arginine vasopressin. Defects must be present somewhere in a vasopressin signal transduction pathway in kidney collecting duct. Recent genetic analysis demonstrated that mutations in vasopressin type 2 receptor and water...

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Source

Identifiers

PMID: 9702064

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-08.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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