Novel Mutant Vasopressin-neurophysin II Gene Associated with Familial Neurohypophyseal Diabetes Insipidus-Reference-Cited by-同舟云学术

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Novel Mutant Vasopressin-neurophysin II Gene Associated with Familial Neurohypophyseal Diabetes Insipidus

Published:2004 Issue:6 Volume:51 Page:551-556
ISSN:0918-8959
Container-title:Endocrine Journal
language:en
Short-container-title:Endocr J

Author:

MIYAKOSHI Masashi¹,KAMOI Kyuzi¹,MURASE Takashi²,SUGIMURA Yoshihisa²,OISO Yutaka³

Affiliation:

1. Department of Internal Medicine, Division of Endocrine and Metabolism, Nagaoka Red Cross Hospital

2. Department of Teratology and Genetics, Research Institute of Environmental Medicine, Nagoya University

3. Department of Endocrinology and Diabetology, Nagoya University, School of Medicine

Publisher

Japan Endocrine Society

Subject

Endocrinology,Endocrinology, Diabetes and Metabolism

Link

http://www.jstage.jst.go.jp/article/endocrj/51/6/51_6_551/_pdf

Reference23 articles.

1. Human Gene Mutation Database?A biomedical information and research resource

2. A single base substitution in the coding region for neurophysin II associated with familial central diabetes insipidus.

3. Identification of a novel mutation in the arginine vasopressin-neurophysin II gene in familial central diabetes insipidus

4. A missense mutation encoding Cys73Phe in neurophysin II is associated with autosomal dominant neurohypophyseal diabetes insipidus

Cited by 11 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Central Diabetes Insipidus Caused by Arginine Vasopressin Gene Mutation: Report of a Novel Mutation and Review of Literature;Hormone and Metabolic Research;2020-07-06

2. Genetics of Diabetes Insipidus;Endocrinology and Metabolism Clinics of North America;2017-06

3. Hypernatremic States;Seldin and Giebisch's The Kidney;2013

4. Nonobstructive hydronephrosis due to social polydipsia: a case report;Journal of Medical Case Reports;2012-11-06

5. Growth retardation in untreated autosomal dominant familial neurohypophyseal diabetes insipidus caused by one recurring and two novel mutations in the vasopressin-neurophysin II gene;European Journal of Endocrinology;2011-02

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