Forty-One Individuals With Mutations in the AVP-NPII Gene Associated With Familial Neurohypophyseal...
Forty-One Individuals With Mutations in the AVP-NPII Gene Associated With Familial Neurohypophyseal Diabetes Insipidus
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Full title
Author / Creator
Familial neurohypophyseal diabetes insipidus Spanish working group , García-Castaño, Alejandro , Madariaga, Leire , Pérez de Nanclares, Gustavo , Vela, Amaia , Rica, Itxaso , Gaztambide, Sonia , Martínez, Rosa , Martinez de LaPiscina, Idoia , Urrutia, Inés , Aguayo, Anibal , Velasco, Olaia and Castaño, Luis
Publisher
US: Oxford University Press
Journal title
Language
English
Formats
Publication information
Publisher
US: Oxford University Press
Subjects
More information
Scope and Contents
Contents
Abstract
Context
Familial neurohypophyseal diabetes insipidus is a rare disease produced by a deficiency in the secretion of antidiuretic hormone and is caused by mutations in the arginine vasopressin gene.
Objective
Clinical, biochemical, and genetic characterization of a group of patients clinically diagnosed with familial neurohypoph...
Alternative Titles
Full title
Forty-One Individuals With Mutations in the AVP-NPII Gene Associated With Familial Neurohypophyseal Diabetes Insipidus
Authors, Artists and Contributors
Identifiers
Primary Identifiers
Record Identifier
TN_cdi_proquest_miscellaneous_2354735511
Permalink
https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_proquest_miscellaneous_2354735511
Other Identifiers
ISSN
0021-972X
E-ISSN
1945-7197
DOI
10.1210/clinem/dgaa069
