Impaired trafficking of mutated AVP prohormone in cells expressing rare disease genes causing autosomal dominant familial neurohypophyseal diabetes insipidus-Reference-Cited by-同舟云学术

Impaired trafficking of mutated AVP prohormone in cells expressing rare disease genes causing autosomal dominant familial neurohypophyseal diabetes insipidus

Published:2004-01 Issue:1 Volume:60 Page:125-136
ISSN:0300-0664
Container-title:Clinical Endocrinology
language:en
Short-container-title:Clin Endocrinol

Author:

Christensen Jane H.,Siggaard Charlotte,Corydon Thomas J.,Robertson Gary L.,Gregersen Niels,Bolund Lars,Rittig Soren

Publisher

Wiley

Subject

Endocrinology, Diabetes and Metabolism,Endocrinology

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1365-2265.2004.01953.x/fullpdf

Reference46 articles.

1. Hereditary diabetes insipidus: an immunohistochemical study of the hypothalamus and pituitary gland

2. Mechanism of Endoplasmic Reticulum Retention of Mutant Vasopressin Precursor Caused by a Signal Peptide Truncation Associated with Diabetes Insipidus

3. Determinants of the natriuresis after acute, slow sodium loading in conscious dogs

4. Hereditary Idiopathic Diabetes Insipidus

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