Response to Letter to the Editor: "Forty-One Individuals with Mutations in the AVP-NPII Gene Associated with Familial Neurohypophyseal Diabetes Insipidus

J Clin Endocrinol Metab. 2020 Jul 1;105(7):dgaa255. doi: 10.1210/clinem/dgaa255.

Authors

Alejandro García-Castaño¹, Leire Madariaga^{1

2

3}, Gustavo Pérez de Nanclares^{1

2}, Amaia Vela^{1

2

3}, Itxaso Rica^{1

2}, Sonia Gaztambide^{1

2

3}, Rosa Martínez¹, Idoia Martinez de LaPiscina¹, Inés Urrutia¹, Anibal Aguayo^{1

2}, Olaia Velasco¹, Luis Castaño^{1

2

3}

Affiliations

¹ Biocruces Bizkaia Health Research Institute, CIBERDEM, CIBERER, Barakaldo, Spain.
² Hospital Universitario Cruces, Barakaldo, Spain.
³ UPV/EHU, Leioa, Spain.

PMID: 32392319
DOI: 10.1210/clinem/dgaa255

No abstract available

Keywords: AVP-NPII gene; familial neurohypophyseal diabetes insipidus.

Publication types

Letter
Research Support, Non-U.S. Gov't
Comment

MeSH terms

Diabetes Insipidus*
Diabetes Insipidus, Neurogenic* / genetics
Diabetes Mellitus*
Humans
Mutation
Neurophysins / genetics

Substances

Neurophysins