Progressive decline of vasopressin secretion in familial autosomal dominant neurohypophyseal diabetes insipidus presenting a novel mutation in the vasopressin-neurophysin II gene-Reference-Cited by-同舟云学术

Progressive decline of vasopressin secretion in familial autosomal dominant neurohypophyseal diabetes insipidus presenting a novel mutation in the vasopressin-neurophysin II gene

Published:2003-09-18 Issue:4 Volume:59 Page:511-518
ISSN:0300-0664
Container-title:Clinical Endocrinology
language:en
Short-container-title:

Author:

Elias Paula C. L.,Elias Lucila L. K.,Torres Natalia,Moreira Ayrton C.,Antunes-Rodrigues Jose,Castro Margaret

Publisher

Wiley

Subject

Endocrinology, Diabetes and Metabolism,Endocrinology

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1046/j.1365-2265.2003.01834.x/fullpdf

Reference58 articles.

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2. A missense mutation in the vasopressin-neurophysin precursor gene cosegregates with human autosomal dominant neurohypophyseal diabetes insipidus;Bahnsen;Embo Journal,1992

3. Diabetes insipidus;Baylis;Journal of Royal College Physicians London,1998

4. Vasopressin function in familial cranial diabetes insipidus;Baylis;Postgraduate Medical Journal,1981

5. Mechanism of endoplasmic reticulum retention of mutant vasopressin precursor caused by a signal peptide truncation associated with diabetes insipidus;Beuret;Journal of Biology Chemistry,1999

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