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Article

Autosomal dominant neurohypophyseal diabetes insipidus with linkage to chromosome 20p13 but without mutations in the AVP-NPII gene.

The Journal of clinical endocrinology and metabolism - 1 Jul 2005

Ye Lei, Li Xiaoying, Chen Ying, Sun Hongtao, Wang Weiqing, Su Tingwei, Jiang Lei, Cui Bin, Ning Guang

Abstract excerpt

CONTEXT: Autosomal dominant neurohypophyseal diabetes insipidus (ADNDI) has been known as a rare disorder transmitted as an autosomal dominant trait, characterized by polyuria and polydipsia, and caused by deficient neurosecretion of arginine vasopressin precursor (AVP-NPII). We reported an ADNDI family with linkage to chromosome 20p13 but without mutations in the AVP-NPII gene. OBJECTIVE: The objective of this...

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Source

Identifiers

PMID: 15811933
DOI: 10.1210/jc.2004-2000

Genes

AVP

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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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Autosomal dominant neurohypophyseal diabetes insipidus with linkage to chromosome 20p13 but without mutations in the AVP-NPII gene.PMID 15811933Read ↗

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