Response to Letter to the Editor: “Forty-One Individuals with Mutations in the AVP-NPII Gene Associated with Familial Neurohypophyseal Diabetes Insipidus
- 11 May 2020
- journal article
- letter
- Published by The Endocrine Society in Journal of Clinical Endocrinology & Metabolism
- Vol. 105 (7), e2687-e2688
- https://doi.org/10.1210/clinem/dgaa255
Abstract
Alejandro García-Castaño, Leire Madariaga, Gustavo Pérez de Nanclares, Amaia Vela, Itxaso Rica, Sonia Gaztambide, Rosa Martínez, Idoia Martinez de LaPiscina, InKeywords
Funding Information
- Department of Health, Australian Government (2018111097, 2017111014)
This publication has 3 references indexed in Scilit:
- The Novel Ser18del AVP Variant Causes Inherited Neurohypophyseal Diabetes Insipidus by Mechanisms Shared with Other Signal Peptide VariantsNeuroendocrinology, 2017
- Identification of five novel arginine vasopressin gene mutations in patients with familial neurohypophyseal diabetes insipidusInternational Journal of Molecular Medicine, 2016
- Early-onset central diabetes insipidus is associated with de novo arginine vasopressin–neurophysin II or Wolfram syndrome 1 gene mutationsActa Endocrinologica, 2015