A Novel Deletion Mutation of the Arginine Vasopressin Receptor 2 Gene in a Japanese Infant with Nephrogenic Diabetes Insipidus

Detalles Bibliográficos
Autores principales: Daitsu, Takashi, Igaki, Junko, Goto, Masahiro, Hasegawa, Yukihiro
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Japanese Society for Pediatric Endocrinology 2014
Materias:
Mutation-in-Brief
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4219939/
https://www.ncbi.nlm.nih.gov/pubmed/25374441
http://dx.doi.org/10.1297/cpe.23.115
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author Daitsu, Takashi
Igaki, Junko
Goto, Masahiro
Hasegawa, Yukihiro
author_facet Daitsu, Takashi
Igaki, Junko
Goto, Masahiro
Hasegawa, Yukihiro
author_sort Daitsu, Takashi
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spelling pubmed-42199392014-11-05 A Novel Deletion Mutation of the Arginine Vasopressin Receptor 2 Gene in a Japanese Infant with Nephrogenic Diabetes Insipidus Daitsu, Takashi Igaki, Junko Goto, Masahiro Hasegawa, Yukihiro Clin Pediatr Endocrinol Mutation-in-Brief The Japanese Society for Pediatric Endocrinology 2014-11-06 2014-10 /pmc/articles/PMC4219939/ /pubmed/25374441 http://dx.doi.org/10.1297/cpe.23.115 Text en 2014©The Japanese Society for Pediatric Endocrinology http://creativecommons.org/licenses/by-nc-nd/3.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution Non-Commercial No Derivatives (by-nc-nd) License.
spellingShingle Mutation-in-Brief
Daitsu, Takashi
Igaki, Junko
Goto, Masahiro
Hasegawa, Yukihiro
A Novel Deletion Mutation of the Arginine Vasopressin Receptor 2 Gene in a Japanese Infant with Nephrogenic Diabetes Insipidus
title A Novel Deletion Mutation of the Arginine Vasopressin Receptor 2 Gene in a Japanese Infant with Nephrogenic Diabetes Insipidus
title_full A Novel Deletion Mutation of the Arginine Vasopressin Receptor 2 Gene in a Japanese Infant with Nephrogenic Diabetes Insipidus
title_fullStr A Novel Deletion Mutation of the Arginine Vasopressin Receptor 2 Gene in a Japanese Infant with Nephrogenic Diabetes Insipidus
title_full_unstemmed A Novel Deletion Mutation of the Arginine Vasopressin Receptor 2 Gene in a Japanese Infant with Nephrogenic Diabetes Insipidus
title_short A Novel Deletion Mutation of the Arginine Vasopressin Receptor 2 Gene in a Japanese Infant with Nephrogenic Diabetes Insipidus
title_sort novel deletion mutation of the arginine vasopressin receptor 2 gene in a japanese infant with nephrogenic diabetes insipidus
topic Mutation-in-Brief
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4219939/
https://www.ncbi.nlm.nih.gov/pubmed/25374441
http://dx.doi.org/10.1297/cpe.23.115
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