Identification of a novel X-linked arginine-vasopressin receptor 2 mutation in nephrogenic diabetes insipidus
Author:
Publisher
Ovid Technologies (Wolters Kluwer Health)
Subject
General Medicine
Reference27 articles.
1. Hereditary nephrogenic diabetes insipidus in Japanese patients: analysis of 78 families and report of 22 new mutations in AVPR2 and AQP2;Sasaki;Clin Exp Nephrol,2013
2. Identification and characterization of a novel X-linked AVPR2 mutation causing partial nephrogenic diabetes insipidus: a case report and review of the literature;Neocleous;Metabolism,2012
3. X-linked nephrogenic diabetes insipidus: from the ship Hopewell to RFLP studies;Bichet;Am J Hum Genet,1992
4. A novel AVPR2 missense mutation in a Chinese boy with severe inherited nephrogenic diabetes insipidus;Huang;J Pediatr Endocrinol Metab,2011
5. Molecular biology of hereditary diabetes insipidus;Fujiwara;J Am Soc Nephrol,2005
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