A Novel Mutation of the Vasopressin-Neurophysin II Gene in a Familial Neurohypophyseal Diabetes Insipidus
Author:
Affiliation:
1. Department of Internal Medicine, Hallym University School of Medicine, Korea.
2. Department of Internal Medicine, KyungHee University College of Medicine, Korea.
Publisher
Korean Endocrine Society
Link
https://synapse.koreamed.org/pdf/10.3803/jkes.2007.22.2.118
Reference20 articles.
1. Pituitary Hyperplasia Secondary to Hypothyroidism Caused by Hashimoto's Thyroiditis in a Female Adolescent
2. Mutant Vasopressin Precursors That Cause Autosomal Dominant Neurohypophyseal Diabetes Insipidus Retain Dimerization and Impair the Secretion of Wild-type Proteins
3. Heterologous Expression of Human Vasopressin-Neurophysin Precursors in a Pituitary Cell Line: Defective Transport of a Mutant Protein from Patients with Familial Diabetes Insipidus
4. A diabetes insipidus vasopressin prohormone altered outside the central core of neurophysin accumulates in the endoplasmic reticulum
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